Community Blood Centers of South Florida, Inc.
Blood products, for which RBC volume QC. failed, were distributed.
Blood Bank of San Bernardino and Riverside Counties
Blood product, possibly contaminated with air, was distributed.
Blood products, which were not quarantined subsequent to receiving information regarding a post donation information related to vCJD risk, were distributed.
Tri-Counties Blood Bank dba UBS- Central Coast
Blood products, collected from a donor who traveled to a malarial endemic area, were distributed.
Blood product, positive for the c-antigen but labeled as c-antigen negative, was distributed.
Blood products, which were collected from a donor who traveled to a malarial endemic area, were distributed.
Blood products,  that were possibly contaminated with Enterococcus Faecalis, were distributed.
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Blood product,  which was positive for E antigen was distributed to a recipient who was identified  with an E antibody.
Blood product, collected from a deferred donor who was improperly re-entered, was distributed.
Blood and Blood Products for Reprocessing
Blood products, collected from a donor in whom donor suitability was not adequately determined, were distributed.
Blood products, which were collected from a donor in which donor suitability was not adequately determined, were distributed.
Blood products, collected from donors for whom donor suitability was not adequately determined, were distributed.
Blood products, collected from donors, whose suitability to donate was not adequately determined, were distributed.
Platelets Pheresis Leukocytes Reduced Irradiated
Blood product, manufactured from a unit of whole blood with incorrect volume was distributed.
Blood product, collected from a donor, whose suitability to donate was not adequately determined, was distributed.
Blood products, collected from donors who were permanently deferred, were distributed.
Blood products, collected from donors whose suitability to donate were not adequately determined, were distributed.
Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Worldwide Distribution - USA Nationwide including Puerto Rico and countries of: Austria, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Luxembourg, Martinique, Mexico, Netherlands, Poland, Russian Federal, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey and United Kingdom.
Eon and Eon Mini charging system, model numbers Eon -3701 (Wall Charger), 3711 (Portable Charger) and Eon Mini -3721 (Charger);  This is a continuation of the firm's July 2012 recall.   Product Usage:  The Eon Wall Charger (3701) provides the capability to recharge the IPG Battery. The charger transmits RF energy through the antenna to the IPG battery to recharge it. The Eon Portable Charger (3711) provides the capability to recharge the IPG battery. The charger transmits RF energy through the antenna to the IPG battery to recharge it. The patient can be mobile during the recharging process with a portable charger. The Eon Mini Charger (3721) provides the capability to recharge the IPG battery while stimulation is either on or off. The charger transmits RF energy through the antenna to the IPG battery to recharge it.
There is issues of warmth or heating at the implant site during charging for the Eon Mini implantable pulse generators (IPGs).  In the July 2012 letter St. Jude Medical informed customers that they would be implementing design improvements to the charger to address possible increased energy dissipation when the charger is misaligned with the IPG or the IPG is implanted too near the surface of the skin.  This field action is to announce the availability of the newly designed Eon Mini Charger Model 3722 to mitigate excessive heating while charging.
Nationwide and Military and Government Consignees
Mitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits per box (NDC 49771-002-03), Rx only, Manufactured for: Mobius Therapeutics, LLC, 4041 Forest Park Avenue, St. Louis, MO  63108 USA.
Non-Sterility: one or more components of the kit have been found to be contaminated with yeast.
Nature's Deli Chicken Jerky Dog Treats, 2.5 lbs. bag, UPC 647263800208, 3 lbs UPC 647263800215, Division of Kasel Industries, Denver, CO 80205. Packaged in a transparent, flexible, plastic bag; the bag is yellow with black and white print writing and a photograph of a golden retriever dog on it.
Best By dates of 04202013 DEN to 10032013 DEN excluding Best By 09192013 DEN, which was recalled on 10/03/2012.
Kasel Industries received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling all lots of pet treats manufactured at their facility between April 20, 2012 and September 19, 2012 due to positive Salmonella findings in the firm's products and facility.
Boots & Barkley Loving your pet from head to tail. Roasted American Pig Ears. Delicious Treat for Dogs, Made in the U.S.A. Distributed by TARGET Corporation, Minneapolis, MN 55403, net wt 12 oz, 12 count, UPC 647263899158.
Best By dates of 20APR2014 DEN to 03OCT2014 DEN, excluding Best By 13SEP2014DEN, which was recalled on 10/17/2012.
Boots & Barkley Loving your pet from head to tail. American Variety Pack Real Beef & Pork. Treats for Dogs. Product of U.S.A. Distributed by TARGET Corporation, Minneapolis, MN 55403, net wt 32 oz. Packaging is white, blue and red with red, black and blue print writing, UPC 490830400086.
Best by dates of 20APR2014 DEN to 03OCT2014 DEN, excluding Best By 13SEP2014DEN, which was recalled on 10/17/2012.
Boots & Barkley American Beef Bully Stick, 12 inch.  Satisfies your dog's instinctive urge to chew. Ingredients: Beef Pizzles. Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239043165.
Best By dates of 20APR2014 DEN to 03OCT2014 DEN.
Boots & Barkley American Smoked Beef Femur Bone 3 inch.  Satisfies your dog's instinctive urge to chew. Ingredients: Beef Femur Bone. Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239403495.
Boots & Barkley American Beef Tendon Flossie 6-8 inch.  Satisfies your dog's instinctive urge to chew. Ingredients: Beef Tendon. Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239043103.
Boots & Barkley American Pig Ear Strips 8 oz.  Satisfies your dog's instinctive urge to chew. Ingredients: Pig Ears. Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239403440.
Boots & Barkley Chicken Stuffed American Beef Femur Bone, 6 inch.  Satisfies your dog's instinctive urge to chew. Ingredients: Beef Femur Bone Chicken Breast, Natural Flavorings. Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239043202.
Boots & Barkley American Braided Beef Bully Stick, 5 inch.  Satisfies your dog's instinctive urge to chew. Ingredients: Beef Pizzles.  Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is transparent with white, blue and red with red, black and blue print writing on the affixed label, UPC 085239043110.
Boots & Barkley American Chicken Jerky, 16 oz UPC 085239043325; 8 oz UPC 085239043400.  Satisfies your dog's instinctive urge to chew. Ingredients: Chicken Breast, Natural Flavorings.  Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Made in U.S.A.  Packaging is semi-transparent with white, blue and red with red, black and blue print writing on the affixed label.  The labeling also has digital photos of the chicken strips and a picture of a terrier dog.
Boots & Barkley American Beef Knuckle, 14 oz.  Promotes Plaque and Tartar Reduction.  Ingredients: Beef Knuckle.  Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Packaging is semi-transparent with white, blue and red with red, black and blue print writing on the affixed label.  The labeling also has digital photo of a dog. UPC 647263899172.
Boots & Barkley American Pork Femur, 1 bone.  Promotes Plaque and Tartar Reduction.  Ingredients: Pork Femur.  Distributed by TARGET Corporation, Minneapolis, MN 55403, 2012 Target Brands, Inc.  Packaging is semi-transparent with white, blue and red with red, black and blue print writing on the affixed label.  The labeling also has digital photo of a dog.  UPC 647263899165.
BIXBI Skin and Coat Beef Liver Jerky, 5 oz.  Packaged in orange semi-transparent flexible plastic packaging, 100% USA Made and Sourced, UPC 091037018021.
Best By dates of 04202014 DEN to 10032014 DEN.
BIXBI Skin and Coat Lamb Jerky, 5 oz.  Packaged in purple and orange semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018045.
BIXBI Hip and Joint Pork Jerky, 5 oz.  Packaged in yellow and aqua semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018144.
BIXBI Skin and Coat Chicken Breast Jerky Treats, 5 oz.  Packaged in orange and green semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018007.
BIXBI Skin and Coat Pork Jerky, 5 oz.  Packaged in orange and aqua semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018069.
BIXBI Hip and Joint Lamb Jerky, 5 oz.  Packaged in yellow and purple semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018120.
BIXBI Hip and Joint Chicken Breast Jerky, 5 oz.  Packaged in yellow and green semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018083.
BIXBI Hip and Joint Beef Liver Jerky, 5 oz.  Packaged in yellow and red semi-transparent flexible plastic packaging with black and transparent print writing, 100% USA Made and Sourced, UPC 091037018106.
Sam's Club Roasted Pig Ear Dog Treats, 28 oz, UPC 681131857246.
Colorado Naturals Chicken Chips, 16 oz, UPC 647263800291, Distributed by Petco/Kasel Ind.
Colorado Naturals Salmon Jerky, 4 oz UPC 647263900175.  Distributed by Petco/Kasel Industries.
Colorado Naturals Chicken Jerky, 4 oz UPC 647263800178, 16 oz UPC 647263800291.  Distributed by Petco/Kasel/Menards Industries.
Colorado Naturals Lamb Jerky, 4 oz UPC 647263510176, Distributed by Petco/Kasel Industries.
Colorado Naturals Pork Jerky, 16 oz UPC 647263700157, Distributed by Petco/Kasel Industries/Menards.
Colorado Naturals Beef Jerky, 4 oz UPC 647263801175, Distributed by Petco/Kasel Industries.
TDBBS, Inc/Best Bully Sticks Buffalo Hearts Sliced, 3 lbs, Bulk.
TDBBS, Inc/Best Bully Sticks Knee Caps, 25 ct, Bulk.
TDBBS, Inc/Best Bully Sticks Pork Jerky Strips, 16 oz.
TDBBS, Inc/Best Bully Sticks Chicken Jerky, 16 oz.
TDBBS, Inc/Best Bully Sticks Turkey Cubes, 4.5 oz.
TDBBS, Inc/Best Bully Sticks Pig Snouts, 25 ct, Bulk.
TDBBS, Inc/Best Bully Sticks Beef Lobster Tails, 1ct, Bulk.
TDBBS, Inc/Best Bully Sticks Turkey Jerky Sticks, 6 ct.
TDBBS, Inc/Best Bully Sticks hearts of Lamb, 4 oz.
TDBBS, Inc/Best Bully Sticks Lamb Jerky, 4 oz.
Nutri-Pet 16oz Natural Filet Strips, UPC 76-0081.
K9 Chicken Breath Fresh Jerky 5oz, UPC 669125507100 ; 15oz  , UPC 669125507117
K9 Chicken Senior Jerky 5oz, UPC 669125507124.
K9 Chicken Digestive Jerky 5oz, UPC  669125507148.
K9 Chicken Healthy Weight Jerky 5oz, UPC 669125507162.
K9 Hip & Joint Chicken Strips 8oz, UPC 669125990445
Best By dates of 04202014 DEN to 10032014 DEN
Verve, 4lb box, 6 units/case, Item# V4, UPC 183413000 89 5, and 10 lb box, 4 units/case, Item #VR, UPC 183413000 17 8.
Item Code: V4 + VR, Lot # 2332A (batches 1-3). Item Code: VR, Lot # 3062A (batches 8 & 9).
The Honest Kitchen is recalling five lots of its Verve, Zeal and Thrive pet food products because they have the potential to be contaminated with Salmonella.
Free Thrive, 1 oz. sample, 50 units/case, Item#TMC, UPC 183413000 81 9.
Zeal, 4lb box, 6 units/case, Item#Z4, UPC 18341300195 3, and 10lb box, 4 units/case, Item# ZR, UPC 18341300191 5.
Item Code: Z4 + ZR, Lot # 2272A (batches 1-5). Item Code: ZR, Lot # 2652A (batches 1-4).
Nationwide including Puerto Rico, OUS to include:  Canada, China, Indonesia, Japan, Kuwait, Panama, Pakistan, Singapore, South Korea, United Arab Emirates.
Kaytee Fiesta Max Canary/Finch, Net Wt. 2 lb., UPC 71859-40410
Best Before Code (month/day/year) 9/28/2013 thru 5/7/2014
Kaytee Products is recalling several bird treats and greens items due to possible contamination of Salmonella from parsley flake ingredients supplied to Kaytee by Specialty Commodities, Inc.
Kaytee Honey Treat, Parakeet, Net Wt. 3.5 oz, UPC 71859-00431, 3.5 oz UPC 71859-00434, and 7 oz Value Pack UPC 71859-55027
Best Before Code (month/day/year) 12/4/2013 thru 8/2/2014
Kaytee Fiesta Fruit & Veggie Treat, Parakeet, Net Wt. 3.5 oz, UPC 71859-99885, 9.5 oz UPC 71859-99855,
Best Before Code (month/day/year) 12/18/2013 thru 7/31/2014
Kaytee Forti-Diet Pro Health Honey Treat, Parakeet, Net Wt. 3.5 oz, UPC 71859-94235, 7 oz Value Pack UPC 71859-94236
Best Before Code (month/day/year) 12/4/2013 thru 8/1/2014
Kaytee Forti-Diet Pro Health Munchables Shred-A-Box, Honey Seed Treats, Parakeet, 4 boxes, Net Wt. 2 oz, UPC 71859-94268
Best Before Code (month/day/year) 3/7/2014 thru 7/30/2014
Kaytee Forti-Diet Pro Health Molting & Conditioning, Small Birds, Net Wt. 11 oz, UPC 71859-94264
Best Before Code (month/day/year) 12/25/2013 thru 8/5/2014
Kaytee Fiesta Nutty Papaya Treat, Parakeet & Cockatiel, Net Wt. 2.25 oz, UPC 71859-94368
Best Before Code (month/day/year) 12/4/2013 thru 6/25/2014
Kaytee Fiesta Foraging Treat for Pet Birds, Net Wt. 1.5 oz, UPC 71859-94370
Best Before Code (month/day/year) 1/27/2014 thru 5/29/2014
Grreat Choice Treat Sticks for Small Birds, Net Wt. 3.2 oz, UPC 37257-27166, 9.6 oz, UPC 37257-27165
Best Before Code (month/day/year) 12/10/2013 thru 3/19/2014
Kaytee Foraging Box O' Fun Treat for Pet Birds, Net Wt. 1.5 oz, UPC 71859-94615
Best Before Code (month/day/year) 1/28/2014 thru 7/30/2014
Kaytee Bird Greens Foraging Treat, Net Wt. 1 oz, UPC 71859-94708
Best Before Code (month/day/year) 12/1/2013 thru 5/28/2014
Dog treat products as follows:   a) Jones Natural Chews Co Woofers (beef patties), bulk 50 count box, Item UPC 741956008169  (may be sold individually at retail)    b) Jones Natural Chews Co Woofers (beef patties), 1 pack shrink-wrap, 50 count box, Item UPC 741956008657    c) Jones Natural Chews Co Woofers (beef patties), 1 pack shrink-wrap, 50 count box, Item UPC 741956008183    d) Jones Natural Chews Co Woofers (beef patties) 2 pack shrink-wrap, 25 count box, Item UPC 741956008190
This product is being recalled due to the possible risk of Salmonella.
Press States Nationwide. Distribution List indicates the following:   DE, FL, IL,  IN, ME, MI, NJ, PA, TX, and VA
Magnesium Sulfate 2 grams in Dextrose 5% for Injection, in 50 mL Plastic Infusion Bags, Med Prep Consulting Inc., Tinton Falls, NJ 07712
All Compounded Products, packaged in plastic infusion bags, devices, syringes and glass vials, Med Prep Consulting Inc., Tinton Falls, NJ 07712
Lack of Assurance of Sterility; potential for mold contamination
365 Organic 100% Apple Juice from concentrate with Vitamin C and Calcium in 6.75 fl oz (UPC 0 99482 42095 6) and 64 fl oz. (UPC 0 99482 42096 3) Distributed by:  Whole Foods Market, Austin, TX 78703; 8 units peer shipping case
TX, LA, MD, IN, IL, NE, NC, MN, WI, FL, AL
Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name:  Donut House K -Cup Packs.  12-Count Retail Boxes, Product Code #8934, Donut House Decaffeinated K-Cup Packs
288,144 kcups/4,002 master cases (6 retail boxes per case)/ 24,012 retail boxes
Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.
Hoxworth Blood Center  UC Medical Center
Red Blood Cells (Apheresis) Leukocytes Reduced
Blood product, which was collected from a donor who traveled to a malarial endemic area, was distributed.
Blood products, collected from a donor who did not have a complete physical examination, were distributed.
Northern California Community Blood Bank
Blood products, which were labeled as leukoreduced, but were not tested to verify the White Blood Cell count, were distributed
VIVITROL (naltrexone for extended-release injectable suspension) a) 380 mg vial NDC 65757-303-02, b) 380 mg vial in kit NDC 65757-300-01, Rx Only Manufactured and marketed by Alkermes, Inc., Waltham, MA 02451,
Individual vial lot 402-3683AA, EXP 10/13; kit vial lot 2011-003, EXP 08/13
Lack of Assurance of Sterility: Product did not meet the criteria for container closure integrity testing during routine 24 month stability testing.
Blood products, which were not manufactured in accordance to acceptable product specifications, were distributed.
Blood products, collected from a donor who traveled to an area considered endemic for malaria, were distributed.
Northern Illinois Blood Bank dba Rock River Valley BC
Blood product, collected from a donor who traveled to an area considered endemic for malaria, was distributed.
Worldwide Distribution - USA Nationwide to all fifty (50) states, and internationally including the following countries: ARGENTINA, ARGENTINA, BAHRAIN, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CYPRUS, ECUADOR, EGYPT, EL SALVADOR, GREECE, HONDURAS, INDIA, INDONESIA, ISRAEL, JAMAICA, JAPAN, JORDAN, KOREA, REPUBLIC OF, KUWAIT, LEBANON, MEXICO, NETHERLANDS ANTILLES, NICARAGUA, PAKISTAN, PANAMA, PARAGUAY, PERU, PHILIPPINES, PUERTO RICO, QATAR, RUSSIAN FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, TAIWAN, PROVINCE OF CHINA, THAILAND, TRINIDAD AND TOBAGO, TURKEY, UNITED ARAB EMIRATES, URUGUAY, VENEZUELA and YEMEN.
LIGACLIP Endoscopic Rotating Multiple Clip Applier (ER320), 10mm M/L    Product Usage:  The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a sterile, single patient use instrument designed to provide a means of ligation through ENDOPATH surgical trocars. The instrument delivers 20 titanium clips that individually advance after each firing. The shaft is made of a low glare material that minimizes reflective distortion. It is designed to rotate 360 in either direction. The rotating knob is located to allow for a one-handed technique.
Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP 10mm M/L Endoscopic Rotating Multiple Clip Applier (ER320) due to potential clip formation and feeding issues which may result in improper clip formation, vessel damage and/or insufficient occlusion of the vessel or other structure
LIGACLIP Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex Trays), 10mm M/L    Product Usage:  The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a sterile, single patient use instrument designed to provide a means of ligation through ENDOPATH surgical trocars. The instrument delivers 20 titanium clips that individually advance after each firing. The shaft is made of a low glare material that minimizes reflective distortion. It is designed to rotate 360 in either direction. The rotating knob is located to allow for a one-handed technique.
LIGACLIP Endoscopic Rotating Multiple Clip Applier (ER320), 10mm M/L, bulk non-sterile   Product Usage:  The LIGACLIP Endoscopic Rotating Multiple Clip Applier is a single patient use instrument designed to provide a means of ligation through ENDOPATH surgical trocars. The instrument delivers 20 titanium clips that individually advance after each firing. The shaft is made of a low glare material that minimizes reflective distortion. It is designed to rotate 360 in either direction. The rotating knob is located to allow for a one-handed technique.
Red Blood Cells Leukocytes Reduced Irradiated
Blood product, which was  irradiated but labeled with incorrect irradiation status and expiration date, was distributed.
Blood product, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.
Blood product, collected from an ineligible donor, was distributed.
Blood products, in which quality control and distribution of products did not meet specifications, were distributed.
Carter BloodCare/ WE & Lela I Stewart Blood Center, Inc
Nationwide & Bahamas, Barbados, Bermuda, Japan
Pharmalucence Kit for the Preparation of Technetium Tc 99m Sestamibi Injection for Mycardial and Breast Imaging. For Intravenous Use and Reconstitution. a) Five vials kits: NDC# 45567-0555-1, b) Thirty vials kits: NDC# 45567-0555-2,  Rx Only, Manufactured by: Pharmalucence, Inc., Billerica, MA 01821
Presence of Particulates; particulate found in retain sample
Worldwide distribution: USA (nationwide) and countries of: Canada, Columbia, Nigeria, Kuwait and Saudi Arabia.
TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum Complete mattress, and AccuMax Quantum Convertible mattress    The TotalCare Bed System is intended to provide a patient support ideally suited to be used in health care environments. The TotalCare Bed System may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post anesthesia care unit (PACU), and sections of the emergency department (ED). The TotalCare Bed System is capable of being used with a broad patient population as determined appropriate by the caregiver or institution.
Bed model numbers: PAU001010784, PAU005010784, P1900, PAK169N10184, PAK169N10384, PA8171210184, PA8175210184, PA8175210384, PA8171210384, PA8171310384, and PA8173210384.    The AccuMax Quantum VPC, Complete and Convertible mattresses are not serialized, but were distributed between September 2005 and April 2013
Hill-Rom is initiating this recall due to a potential issue with TotalCare Beds equipped with AccuMax Quantum'' mattresses. If the bed is put into the chair egress position, the magnets on the mattress may not hold the bottom of the mattress flat to the bed frame. If this happens, the foot section of the mattress will extend away from the bed at about a 30 angle (as shown in the photo). A patient attempting to get back into the bed may assume that the mattress is against the bed and attempt to sit, but may miss the seat and sit on the foot section instead. This can result in the patient sliding down to the floor, with possible injury. If the patient falls, the result may be major critical muscular/skeletal injury.
Nationwide distribution: US including states of:  AL, CA, CO, FL, GA, ID, KY, MD, NC, NJ, NY, OH, PA, TN, VA, and WA.
Advanced Orthogonal Percussion Adjusting Instrument    Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
Worldwide Distribution- US (nationwide) including states of: MA, ME, CT, NJ, NY, PA, MD, VA, NC, SC, GA, FL, AL, TN, MS, KY, OH, IN, MI, IA, WI, MN, SD, MT, IL, MO, KS, NE, LA, AR, OK, TX, CO, ID, AZ, CA, OR, WA, AK, RI, VT and the countries of: Angola, Argentina, Australia, Austria, Belgium, Bermuda, Brazil, Bulgaria, Canada, Caribbean, Chile, Colombia, Costa Rica, Czech, Denmark, Dubai, Ecuador, Egypt, France, Germany, Gibraltar, Great Britain, Greece, Guatemala, Hungary, India, Indonesia, Iran, Israel, Italy, Jamaica, Jordan, Korea, Kossovo, Kuwait, Lebanon, Lithuania, Malaysia, Malta, Mexico, Morocco, Netherlands, Norway, Panama, Peru, Philippines, Poland, Portugal, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Syria, Taiwan, Thailand, Trinidad, Turkey, Ukraine, Uruguay, Vietnam, and Japan.
HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluation of the extrinsic coagulation pathway and the monitoring of Oral Anticoagulant Therapy.
Instrumentation Laboratory is recalling HemosIL RecombiPlasTin 2G (RPT2G), Part No. 0020009580 (8 mL Size) due to being Out of Specification.
International distribution: Austria, Australia, Belgium, Brazil, Canada, Czech Republic, Denmark, Esonia, Finland, France, Great Britain, Germany, Greece, Hong Kong, Ireland, Isreal, Iceland, Italy, Kingdom of Bahrain, Kuwait, Lithuania, Netherlands, Norge, New Zealand, Spain, Switzerland, Sweden, and United Arab Emirates.
Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt shower chair.   Height adjustable four wheeled shower chairs for persons of various weights.
Affected Serial numbers: 3829 to 11028 (same series for all Swift Mobil products)
Etac is voluntarily conducting a field correction of the Etac Swift Mobil shower chair. If the Swift Mobil shower chair loses a caster and thus becomes instantly unstable, there is potiential risk for harm or injury.
West-ward Belladonna Alkaloids with Phenobarbital Tablets, a) 1000-count bottle (NDC 0143-1140-10), b) 5000-count bottle (NDC 0143-1140-51), Rx only, Manufactured by West-ward Pharmacuetical Corp., Eatontown, N.J., 07724
Presence of Foreign Substance: Uncharacteristic blacks spots were found in tablets.
West-ward Belladonna Alkaloids with Phenobarbital Tablets, a) 1000-count bottle (NDC 0143-1140-10),Rx only, Manufactured by West-ward Pharmacuetical Corp., Eatontown, N.J., 07724
Cross contamination with other products: Belladonna Alkaloids with Phenobarbital Tablets contained a  trace amount of Methocarbamol.
IL, IN, IA, KS, MN, NJ, NY, NC, OH, SC, TX, VT.
Vanilla almond granola, Net WT 16 oz(454g), UPC 0 71725 71239 4, Distributed by American Importing Co., Inc, Minneapolis, MN 55414.   Vanilla Almond Granola, Net Wt 16 oz (454g), UPC 7 25439 20038 7,  Distributed by DZA Brands LLC, Salisbury,NC 28147.    Hy-Vee Granola Vanilla Almond, 24 oz,  UPC 71725 71239    Amport, Granola, Vanilla Almond, 22 oz, UPC 71725 72512
American Importing Co., d/b/a Amport Foods is voluntarily recalling a limited number of packages of its Amport Foods 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter from a 3rd party vendor.
Orchard Reserve, Fiber Health Blend, Net WT 6.5 oz , UPC 0 71725 74211 7, Distributed by Amport Foods, Minneapolis, MN 55414.
Smart Sense Fruit & Granola Trail Mix, Net WT 4.0 oz , UPC 8 83967 29091 8, Distributed by Kmart corporation, Hoffman Estates, Il 60179, Minneapolis, MN 55414.
Blood Bank software Primary Application with Model numbers 5.4.0.2 and 5.4.1.
Blood Bank software Primary Application (Model Numbers 5.4.0.2 and 5.4.1), with a defect or glitch, was distributed.
BDTM Stem Cell Control Kit;   BD Biosciences  2350 Qume Drive, San Jose, CA 95131
Catalog number: 340991 Lot numbers: BC053, expires 06/02/13 and BC063, expires 07/02/13.
BD Stem cells controls, not functioning as intended, were distributed.
Worldwide Distribution - USA (nationwide) and countries of: AFGHANISTAN ALBANIA ARGENTINA ARUBA AUSTRALIA AUSTRIA AZERBAIJAN BAHRAIN BANGLADESH BELGIUM BOLIVIA BOSNIA AND HERZEGOWINA BRAZIL BRUNEI DARUSSALAM BULGARIA CAMBODIA CHILE CHINA COLOMBIA COSTA RICA CROATIA (local name: Hrvatska) CYPRUS CZECH REPUBLIC DENMARK ECUADOR EGYPT EL SALVADOR ESTONIA ETHIOPIA FINLAND FRANCE GERMANY GREECE GUADELOUPE HONG KONG ICELAND INDIA INDONESIA IRAQ IRELAND ISRAEL ITALY JAPAN JORDAN KAZAKHSTAN KENYA KOREA, REPUBLIC OF KUWAIT LAOS LATVIA LEBANON LIBYAN ARAB JAMAHIRIYA LITHUANIA LUXEMBOURG MACAU MACEDONIA MALAYSIA MALTA MEXICO MONGOLIA MOROCCO NAMIBIA NEPAL NETHERLANDS NETHERLANDS ANTILLES NEW CALEDONIA NEW ZEALAND NICARAGUA NIGERIA NORWAY OMAN PAKISTAN PALESTINE PANAMA PAPUA NEW GUINEA PARAGUAY PERU PHILIPPINES POLAND PORTUGAL PUERTO RICO QATAR REUNION ROMANIA RUSSIAN FEDERATION SAUDI ARABIA SERBIA SINGAPORE SLOVENIA SOUTH AFRICA SPAIN SRI LANKA SWEDEN SWITZERLAND TAIWAN, PROVINCE OF CHINA TANZANIA, UNITED REPUBLIC OF THAILAND TRINIDAD AND TOBAGO TUNISIA TURKEY UGANDA UKRAINE UNITED ARAB EMIRATES UNITED KINGDOM UZBEKISTAN VENEZUELA VIET NAM and YEMEN.
Philips HeartStart MRx  Monitor/Defibrillator, Model numbers M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6    The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician
Serial numbers ranging from: US00100100 to US00567299 (serial numbers of the HeartStart MRx monitor/defibrillator are printed on the primary label on the back of the MRx in battery bay B)
The MRx may deliver a non-synchronized cardioversion shock resulting in the delivery of incorrect therapy, which may induce ventricular fibrillation.
Worldwide distribution: US (nationwide) including states of: AL, CA, CO, CT, FL, GA, IA, ID, IL, LA, MA, MN, MO, MS, NE, NJ, NY, OH, PA, SC, TN, TX, VA, WA, and WI; and countries of: Canada, Brazil, Malaysia, and Mexico.
Dermalight 80 Model Number UVB-080, one unit per box.    The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.
The following batch numbers and serial numbers are affected by this recall: Batches 7839 and 7951, Serial numbers D80-12748 to D80-12871.
The incorrect manual may have been packaged with this product. UVB-080 devices may have included the manual for a UVA-083 device.
US distribution including the states of: AL, CA, MN, and NC.
Dermalight 80 Model Number UVB-083, one unit per box.   The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.
The following batch and serial numbers are affected by the recall: Batch 007778, Serial numbers D83-30016 to D83-30021.
The incorrect manual may have been packaged with this  product. UVB-083 devices may have included the manual for a UVA-080 device.
AmBisome (amphotericin B) liposome for injection, 50mg vial, single use vial, For Intravenous Infusion Only, Rx Only, Marketed by: Astellas Pharma US, Inc., Northbrook, IL 60062, Manufactured by: Gilead Sciences, Inc, San Dimas, CA 91773, NDC: 0469-3051-30.
Lot #: 042267AA, Exp July 2015, 042287AA, 042289AA, 042291AA, Exp Aug 2015.   Lot Numbers and Expiry Dates (for Canada distribution).  LOT 042269AA, EXP 07/2015,  LOT 0422C1AA, EXP 11/2015.
Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a voluntary recall on certain lots of AmBisome because the manufacturer has notified Astellas that during a routine simulation of the manufacturing of AmBisome, a bacterial contamination was detected in the media fills.
Worldwide distribution: US (nationwide) including states of:  AK, AL, AR, AZ, CA, CO, CT, FL, GA, lA, ID, IL, IN, KS, KY, LA, MA, MD, ME, Ml, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, & WY and countries of: Canada, Argentina, Australia, Austria, Bahrain, Belgium, Brazil, Canada, Chile, China, Columbia, Czech Republic, Dominican Republic, Ecuador, Egypt, India, Indonesia, Israel, Italy, Jamaica, Japan, Korea, Kuwait, Libya, Malaysia, Mexico, Pakistan, Panama, Philippines, Poland, Puerto Rico, Russia, Singapore, Slovenia, South Africa, Spain, Saudi Arabia, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Uruguay, & Venezuela.
Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved dissectors, suction/irrigation devices, accessory ports, pool/sump devices and stone retrieval cannula, packaged and sterilized individually in a transparent flexible blister sealed to a Tyvek lid. 6 flexible packages are placed into a sales unit carton, with 4 cartons per corrugated shipper.    The Endopath Electrosurgery Probe Plus II system has application in minimally invasive procedures to facilitate tissue dissection, coagulation, irrigation, and fluid evacuation through a common trocar sleeve.
Product Code: EPS01, Exp. Date: 2015 09 through 2018 03; Product Code: EPS02, Exp. Date: 2015 09 through 2018 03; Product Code: EPS03, Exp. Date: 2015 09 through 2018 03; Product Code: EPS04, Exp. Date: 2015 09 through 2018 03; Product Code: EPS05, Exp. Date: 2015 09 through 2018 03; Product Code: EPS06, Exp. Date: 2015 09 through 2018 03; Product Code: EPS07, Exp. Date: 2015 09 through 2018 03; Product Code: EPS08, Exp. Date: 2015 09 through 2018 03; Product Code: EPS10, Exp. Date: 2013 04 through 2018 03; Product Code: EPS11, Exp. Date: 2013 04 through 2018 03; Product Code: EPS12, Exp. Date: 2013 04 through 2018 03 & Product Code: EPS13, Exp. Date: 2013 04 through 2018 03.
The firm is recalling the ENDOPATH Probe Plus II Shafts because the possibility that a tear in the Tyvek packaging  may affect the sterility of the device.
Watson Laboratories, Inc.-(Actavis) - Florida
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60
Failed Tablet/Capsule Specifications: Broken tablets
Myoscience brand iovera Smart Tip, Myoscience Cryo-Touch IV, a Cryogenic Surgical device, REF Catalog Number: STA0311-10.   Product Usage:  The Myoscience Cryo-Touch IV (a.k.a. iovera) is used to destroy tissue during surgical procedures by applying freezing cold. It can also be used to produce lesions in peripheral nervous tissue by the application of cold to the selected site for the blocking of pain. The Cryo-Touch IV (a.k.a. iovera) is not indicated for treatment of central nervous system tissue.
The outer box label of the product was labeled with a down revision label which did not include the US labeling requirements, specifically the symbol descriptors and also the ''Caution: Federal Law (USA) restricts this device to sale by or on the order of a physician.'' This product was previously labeled for EU distribution only.
CA, ID, IL, IN, IA, KS, KY, MI, MN, NV, ND, PA, SD, TN, WI.
601009 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK, UPC 2052601009   601076 ANTIOXIDANT SUPERSTAR MIX 12/6 OZ BERGIN RED BAG, UPC 2052601076    601051 ANTIOXIDANT SUPERSTAR MIX 12/8 OZ CLAMSHELL, UPC 2052601051    601051.03 ANTIOXIDANT SUPERSTAR MIX 12/8 OZ CLAMSHELL KOWALSKI, UPC 2052601051    601049.01 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL, UPC 1115099870    601049.1 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL CUB, IUPAC     601070 ANTIOXIDANT SUPERSTAR MIX 3/5#, UPC 2052601070     601050 ANTIOXIDANT SUPERSTAR MIX 30#, UPC 2052601050    601052 ANTIOXIDANT SUPERSTAR MIX 5#, UPC 2052601052    601069 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB, UPC 2052601069    601069.05 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB FESTIVAL, UPC 2052601069    601054 ANTIOXIDANT SUPERSTAR MX 12/10 OZ BAGLINE, UPC 2052601054      601069.04 ANTIOXIDANT SUPERSTAR MIX 8/10 OZ SQ TUB BOULDER, IUPAC       601048.00 ANTIOXIDANT SUPERSTAR MIX 100/2 OZ FLAT PACK PROMOTIONAL ANTIOXIDANT SUPERSTAR MIX***, UPC  2052601048.    601049.00 ANTIOXIDANT SUPERSTAR MIX 16/6 OZ CLAMSHELL SUPER ANTIOXIDANT MIX***, UPC 2052601049      612150.03 LARGE GIFT BOX KOWALSKIS, UPC 2052612150.
Bergin Fruit and Nut Company is initiating a recall on a number of pistachio products  manufacturing using pistachios supplied by ARO Pistachio Company. The recall was initiated because Salmonella was found in the environment at  the ARO Pistachio Company.
601041 HEALTHY HEART MIX 12/14 OZ TRAY, UPC 2052601041   601078 HEALTHY HEART MIX 12/8 OZ CLAMSHELL, UPC 2052601078    601078.03 HEALTHY HEART MIX 12/8 OZ CLAMSHELL KOWALSKI, UPC 2052601078    601089 HEALTHY HEART MIX 16/6 OZ CLAMSHELL, UPC 2052601089    601089.1 HEALTHY HEART MIX 16/6 OZ CLAMSHELL CUB, UPC 1115099868    601125 HEALTHY HEART MIX 8/10 OZ SQ TUB, UPC 2052601125    601125.04 HEALTHY HEART MIX 8/10 OZ SQ TUB BOULDER, UPC 2052601125    601125.05 HEALTHY HEART MIX 8/10 OZ SQ TUB FESTIVAL, UPC 2052601125    601063 HEALTHY HEART NUT MIX 12/16 OZ BAGLINE, UPC 2052601063    601061.05 HEALTHY HEART NUT MIX 12/16 OZ FESTIVAL, UPC 2052601061    601037 HEALTHY HEART NUT MIX 30#, UPC 2052601037    601038 HEALTHY HEART NUT MIX 5#, UPC 2052601038      601089.01 HEALTHY HEART MIX 16/6 OZ CLAMSHELL, UPC 1115099868    602037 HEALTHY HEART NUT MIX 2/5#, UPC  2052602037    601137.00 HEALTHY HEART MIX 12/7 OZ BERGIN CUSTOM ZIPLOCK POUCH DISCONTINUED HEALTHY HEART MIX***, UPC 2052601137
Bergin Fruit and Nut Company is initiating a recall on a number of pistachio products  manufactured using pistachios supplied by ARO Pistachio Inc. Salmonella was found in the environment at  the ARO Pistachio Inc. company.
604320 LOW GLYCEMIC INSTANT OATMEAL 25#, UPC 2052604320
601180 LOW GLYCEMIC SNACK MIX 12/4 OZ BERGIN RED BAG, UPC 2052601180   601082 LOW GLYCEMIC SNACK MIX 12/8 CLAMSHELL, UPC 2052601082    601082.03 LOW GLYCEMIC SNACK MIX 12/8 CLAMSHELL KOWALSKI, UPC 2052601082    601080 LOW GLYCEMIC SNACK MIX 30#, UPC 2052601080    601084 LOW GLYCEMIC SNACK MIX 5#, UPC 2052601084    601083.04 LOW GLYCEMIC SNACK MIX 8/10 OZ SQ TUB, UPC 2052601083    601083 LOW GLYCEMIC SNACK MIX 8/10 OZ SQ TUB, UPC 2052601083
604293 MEGA OMEGA MIX 12/8 OZ SQ TUB, UPC 2052604293   604293.04 MEGA OMEGA MIX 12/8 OZ SQ TUB BOULDER,  UPC 2052604293    604293.05 MEGA OMEGA MIX 12/8 OZ SQ TUB FESTIVAL, UPC 2052604293    604290 MEGA OMEGA MIX 15#, UPC 2052604290     604292 MEGA OMEGA MIX 16/7 OZ - CLAMSHELL,UPC 2052604292    604291 MEGA OMEGA MIX 5#, UPC 2052604291
601911 PISTACHIO KERNELS HOT & SPICY 30#, UPC 2052601911   601913 PISTACHIOS HOT AND SPICY 12/5 OZ BERGIN RED BAG, UPC 2052601913
600943 PISTACHIOS KERNELS  RAW 8/11 OZ SQ TUB, UPC 2052600943   601902 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG, UPC 2052601902    601902.09 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG BYERLYS, UPC 2052601902    600899 PISTACHIOS KERNELS RAW 30#, IUPAC     600901 PISTACHIOS KERNELS RAW 5#, UPC 2052600901       600900.05 PISTACHIOS KERNELS RAW 12/16 BAGLINE FESTIVAL, UPC 2052600900.     601902.08 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG LUNDS RAW PISTACHIO KERNELS, UPC 2052601902.
600908.03 PISTACHIOS KERNELS R/S 12/16 OZ TRAY KOWALSKI, UPC 2052600908   600909 PISTACHIOS KERNELS R/S 16/7 OZ CLAMSHELL,  UPC 2052600909    600909.03 PISTACHIOS KERNELS R/S 16/7 OZ CLAMSHELL KOWALSKI, IUPAC     600904 PISTACHIOS KERNELS R/S 30#, UPC 2052600904    600905 PISTACHIOS KERNELS R/S 5#, UPC 2052600905      600906 PISTACHIOS KERNELS R/S 12/16 OZ BAGLINE, IUPAC.
603684 PISTACHIOS S/I/S 12/10 OZ GOLD BAG, UPC 2052603684   600913 PISTACHIOS S/I/S 12/12 OZ BAGLINE, UPC 2052600913    600913.11 PISTACHIOS S/I/S 12/12 OZ BAGLINE AMAZON, UPC 2052600913    600913.07 PISTACHIOS S/I/S 12/12 OZ BAGLINE DISPLAY BOX, UPC 2052600913    600923.05 PISTACHIOS S/I/S 12/12 OZ BAGLINE FESTIVAL, UPC 2052600923    600915 PISTACHIOS S/I/S 12/12 OZ TRAY, UPC 2052600915    603672 PISTACHIOS S/I/S 12/26 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603672    600921 PISTACHIOS S/I/S 12/8 OZ CLAMSHELL, UPC2052600921     603667 PISTACHIOS S/I/S 16/15 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603667    600912 PISTACHIOS S/I/S 25#, UPC 2052600912    600914 PISTACHIOS S/I/S 4/20 OZ TUB, UPC 2052600914    600914.03 PISTACHIOS S/I/S 4/20 OZ TUB KOWALSKI, UPC 2052600914    603677 PISTACHIOS S/I/S 4/36 OZ TIN HOLIDAY CLOSED SLEEVE, UPC 2052603677    603902 PISTACHIOS S/I/S 4/36 OZ TIN HOLIDAY OPEN SLEEVE, UPC2052603902     600911 PISTACHIOS S/I/S 5#, UPC 2052600911    600927.04 PISTACHIOS S/I/S 8/8 OZ SQ TUB BOULDER, UPC 2052600927     600927.05 PISTACHIOS S/I/S 8/8 OZ SQ TUB FESTIVAL, UPC 2052600927    601912 PISTACHIOS S/IS 10/14 OZ TAPE BAG, UPC2052601912     601912.09 PISTACHIOS S/IS 10/14 OZ TAPE BAG BYERLYS, UPC 2052601912      601912.08 PISTACHIOS S/IS 10/14 OZ TAPE BAG LUNDS, UPC 2052601912    603858.00 PISTACHIOS S/I/S 12/26 OZ OPEN SLEEVE IN SHELL PISTACHIOS, UPC 2052603858.
600910 PISTACHIOS SPLITS RAW 30#, UPC 2052600910
Worldwide distribution: USA including PA and countries of: BRAZIL, BULGARIA, FRANCE, GEORGIA, GERMANY, GREECE, ITALY, LEBANON, NETHERLAND, POLAND, SPAIN, and TURKEY.
AlboGraft Knitted with Collagen, Bifurcate 14x08 Catalog Number: AMC1408    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
Lot number/Expiration Date  56890A     2015-04
Blood blushing/leaking from the surface of the graft after implantation
AlboGraft Knitted with Collagen, Straight 15x06 Catalog Number:  AMC1506     AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
Albo Graft Knitted with Collagen, Bifurcate 16x08 Catalog Number: AMC1608    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Bifurcate 18x09 Catalog Number: AMC1809    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Bifurcate 18x10 Catalog Number: AMC1810    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Bifurcate  20x10Catalog Number: AMC2010    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Straight 40x07 Catalog Number: AMC4007    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Straight 40x08 Catalog Number: AMC4008    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Straight 60x06 Catalog Number: AMC6006    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Straight 60x07 Catalog Number: AMC6007    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Knitted with Collagen, Straight 60x08 Catalog Number: AMC6008    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 15x26 Catalog Number: ATC1526    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 15x30 Catalog Number: ATC1530  AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 30x16 Catalog Number: ATC3016    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 30x18 Catalog Number: ATC3018    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 30x24 Catalog Number: ATC3024    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
AlboGraft Woven with Collagen, Straight 30x26 Catalog Number: ATC3026    AlboGraft Vascular Grafts are made of synthetic material and designed to replace sections of damaged or malfunctioning arteries.
Foreign distribution only to France, Italy, Switzerland, Portugal, Denmark,Turkey, Ireland, Norway, Malta, UK, Greece, Belgium, Austria, Germany, India, Hong Kong, Israel, Saudi Arabia, Thailand, UAE, Singapore, Ecuador, Oman, El Salvador, MCF Holland, MSF, France, Ethiopia, Egypt, Argentina, Chile, Brazil, Spain, Finland, Sweden.
AmBisome (amphotericin B) liposome for Injection, 50 mg, For Intravenous Infusion Only, Single-Use Vial, Rx Only, Marketed by: Astellas Pharma US, Inc., Northbrook, IL 60062, Manufactured by: Gilead Sciences, Inc., San Dimas, CA 91773, NDC 0469-3051-30.
Lack of Sterility Assurance; During a routine simulation of the manufacturing of AmBisome, a bacterial contamination was detected in some media fill units. No contaminated batches have actually been identified in the finished product, but there is a possibility of contamination.
Price Chopper Golub Corperisable Warehouse
Price Chopper stores in NY, NH, MA, VT, PA and CT.
Jacqueline's GOURMET COOKIES Almond Bursts COOKIES, Net Wt. 11 oz (8 units total) packed in clear plastic with white labeling----Shelf life is 12 months frozen and 7 days after baked.
103,032 cookies packed into 12,879 11 oz packages  (10,368 cookies held in stock @ Jacqueline's Gourmet)
Jacqueline's GOURMET COOKIES Brownie Burst Cookies, Net Wt. 11 oz (8 units in total) packed in clear plastic with white labeling--Shelf life is 12 months frozen and 7 days after baked.
112,320 cookes packaged into 14,040 11 oz packages
Jacqueline's GOURMET COOKIES Raspberry Burst Cookies, Net Wt. 11 oz (8 units in total) packed in clear plastic with white labeling---Shelf life is 12 months frozen and 7 days after baked.
112, 536 cookies packaged into 14,067 11 oz packages
Worldwide distribution: US (nationwide) including states of: IL, MA, NC, ND, NY, PA, RI, TX, WA,  and WI; and country of: Canada.
The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a patented Shock Advisory System. This software algorithm analyzes the patient's electrocardiographic (ECG) rhythm and indicates whether or not it detects a shockable rhythm.     The LIFEPAK 500 AED is intended for use by personnel who are authorized by a physician/medical director and is intended for use in the pre-hospital and workplace and community environments.
139 total (125 units in the US and 14 units outside US)
The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible to malfunction due to an assembly error. If affected, the malfunction would be the result of internal shorting on a printed circuit board assembly and could render the device inoperable.
USA Nationwide Distribution in the states of CO, KY, LA, VA, and WI.    The affected product was also distributed to Canada.
STERIS Fine Traction Device, one unit per box   Product Usage:  The Fine Traction Device is used to provide traction and enable fine adjustments to traction and orientation of the leg during orthopedic procedures.
A bearing used in the assembly of the Fine Traction Device did not perform successfully in pre-release reliability testing; a replacement bushing passed reliability testing and was  substituted per a change order.  The change order authorized use of the substitute bushing in assembly of the Fine Traction Accessory; however, inadvertently the new part was not implemented.  During complaint evaluation of a Fine Traction Device returned by a Customer it was determined that the original part, the bearing, was used in Fine Traction Devices distributed to Customers.
Worldwide Distribution - US Nationwide including Guam, Puerto Rico and the countries of : Afghanistan, Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Korea (Republic of), Kuwait, Latvia, Lebanon, Lithuania, Malaysia, Malta, Martinique, Mexico, Morocco, Namibia, Netherlands, New Zealand, Norway, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Russia, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, Uruguay, Venezuela, Vietnam.
GE Healthcare Infinia Hawkeye 4 Option For Dual-Head Variable Angle Gamma Camera, Hawkeye Option for Dual-Head Variable Angle Gamma Camera (this includes GE Quasar Nuclear Medicine Systems).  Nuclear Medicine Systems Infinia devices    Product Usage:  The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition types and optional imaging features designed to enhance image quality in Oncology, Cardiology, Neurology and other clinical diagnostic imaging applications.
GE became aware of an incident at a VA Medical Center facility in the US in which a patient died due to injuries sustained while being scanned on an Infinia Hawkeye 4 Nuclear Medicine System.
GE Healthcare Varicam/VG and VG Hawkeye devices   Product Usage:  The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition typed and optional imaging features designed to enhance image quality in Oncology, Cardiology, Neurology and other clinical diagnostic imaging applications. The scanning modes include planar (Static, Multi-gated, Dynamic, Whole body scanning) and tomographic (SPECT, Gated SPECT, Whole body SPECT, Camera based PET). Acquisition types include single and multi-isotope/multi-peak frame/list mode single-photon and positron imaging. Optional imaging-enhancement features include assortment of collimators, gating by physiological signals, real-time automatic body contouring, and CT-based attenuation correction and functional anatomic mapping.
Elscint APEX Helix, dual-head, multi-purpose, Slip-Ring, digital gamma camera    Product Usage:  The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition typed and optional imaging features designed to enhance image quality in Oncology, Cardiology, Neurology and other clinical diagnostic imaging applications. The scanning modes include planar (Static, Multi-gated, Dynamic, Whole body scanning) and tomographic (SPECT, Gated SPECT, Whole body SPECT, Camera based PET). Acquisition types include single and multi-isotope/multi-peak frame/list mode single-photon and positron imaging. Optional imaging-enhancement features include assortment of collimators, gating by physiological signals, real-time automatic body contouring, and CT-based attenuation correction and functional anatomic mapping.
Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system.     Product Usage:  The Brivo NM 615 is an emission computed tomography system intended to detect the location and distribution of gamma ray photon emitting radionuclides in the body and to produce cross-sectional images through computer reconstruction of the data. The Brivo NM 615 system is intended for General Nuclear Medicine imaging procedures using variety of scanning modes supported by various acquisition types. This generic type of device may include signal analysis and display equipment, patient and equipment supports, and accessories.
GE became aware of an incident at a VA Medical Center facility in the US in which a patient died due to injuries sustained while being scanned on an Infinia Hawkeye 4 Nuclear Medicine System.  UPDATE:  On July 03, 2013 GE notified hospitals that they are recalling several Nuclear Medicine Imaging Systems because serious injuries or deaths could occur due to the failure mode associated with this recall.  GE advised hospitals that they cease use of their Nuclear Medicine systems until GE can complete an inspection of the system.  In this second notification GE included all Nuclear Medicine Systems.
Discovery NM 630, dual detector free-geometry integrated nuclear imaging system.     Product Usage:  The GE Discovery NM 630 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting, localizing, diagnosing of diseases and in assessment of organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer.  The system output can also be used by the physician for staging and restaging of tumors, planning, guiding, and monitoring therapy.  The GE Discovery NM 630 system is a Nuclear Medicine (NM) system, which is intended to yield General Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using a variety of scanning modes supported by various acquisition types and imaging features designed to enhance image quality. The scanning modes include planar mode (Static, Multi-gated, Dynamic and Whole body scanning) and tomographic mode (SPECT, Gated SPECT, Whole body SPECT).  The acquisition types include single and multi-isotope/ multi peak frame/list mode single-photon imaging.  The imaging-enhancement features include assortment of collimators, gating by physiological signals, and real-time automatic body contouring.  The GE Discovery NM 630 system may include signal analysis and display equipment, patient and equipment supports, components and accessories.  The system may be used for patients of all ages.
Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging system.      Product Usage:  The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer.  The system output can also be used by the physician for staging and restaging of tumors, planning, guiding, and monitoring therapy.
Optima NM/CT 640     Product Usage:  The GE Optima NM/CT 640 system is intended for General Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.  It includes a general purpose Nuclear Medicine (NM) system using a variety of scanning modes supported by various acquisition types, and a CT component which is intended specifically for enabling attenuation correction and anatomical localization on SPECT studies
Medtronic Preimplantation Test Kit, Catalog No. 21047. The kit is indicated for use with Medtronic CSF-Flow Control Valves and Delta Valves, when a simple preimplantation test is desired to verify that the valve conforms to labeled product specifications.
Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit because the outer carton had expiration dates that were incorrect.  The date on the outer carton is later than the expiration date for one or more of the individually packaged sterile components in the kit.
Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003. The device is used for diagnostic X-ray imaging.
Model Number 5895003 with serial numbers 1052 through 2500.
Siemens issued a Field Safety Notice about the potential hazard to patients or operators when using the function ''table top float'' of the AXIOM Aristos MX. When repositioning a patient lying on the table top and releasing the table top, it is possible that the fingers of the patient or operator are between the table top and the detector tray and if  the table top is moved, the fingers can be squeezed.
Worldwide distribution: US (nationwide) and countries of:Belgium, Canada, Columbia, Mexico, Singapore, and Taiwan.
BD BBL Vancomycin Screen Agar, carton of 10 plates, catalog # 222204, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   Vancomycin Screen Agar is used to test entercocci for resistance to vancomycin and to predict the synergistic activity of this antimicrobial with an aminoglycoside antimicrobial.
Microbiological identification media may exhibit reduced levels of Vancomycin.
BD BBL Schaedler K-V Agar with 5% Sheep Blood, carton of 20 plates, catalog # 221555, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   Vancomycin Screen Agar is used to test entercocci for resistance to vancomycin and to predict the synergistic activity of this antimicrobial with an aminoglycoside antimicrobial.
BD BBL CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin (KV), packaged in cartons of 100 plates, Catalog # 221736, and labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   CDC Anaerobe 5% Sheep Blood Agar with Kanamycin and Vancomycin is used for the selective isolation of fastidious and slow-growing, obligately anaerobic gram-negative bacteria from a variety of clinical and nonclinical materials.
BD BBL Anaerobe CNA Agar with 5% Sheep Blood // Anaerobe Laked Sheep Blood KV Agar, packaged in cartons of 20 plates, Catalog # 297041, and labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   Anaerobe Laked Sheep Blood KV Agar is used in a qualitative procedure for isolation of gram-negative anaerobic bacilli.
BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV, packaged in cartons of 100 plates, Catalog # 297260, and labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   Bacteroides Bile Esculin Agar (BBE) is recommended as a primary isolation medium for the selection and presumptive identification of the B. fragilis group.
BBL Brucella Laked Blood Agar with Kanamycin and Vancomycin (KV), Catalog # 297840, packaged in cartons of 20 plates, labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   Brucella Laked Blood with KV is used for the selective isolation of fastidious and slow growing, obligately anaerobic bacteria from the same specimen.
BD BBL BCYE Selective Agar with PAV, Catalog # 297880, packaged in cartons of 10 plates, and labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   BCYE Selective with PAV is used in qualitative procedures for isolation of Legionella species from clinical specimen and nonclinical (environmental) samples. It is similar to the Edelstein formula, except that the concentration of polymyxin B is reduced by half, and vancomycin is substituted for cefamandole.
BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium), Catalog # 299614, packaged in cartons of 20 plates, and labeled in part ***Becton, Dickinson and Company  7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds***   BCYE Selective with PAV is used in qualitative procedures for isolation of Legionella species from clinical specimen and nonclinical (environmental) samples. It is similar to the Edelstein formula, except that the concentration of polymyxin B is reduced by half, and vancomycin is substituted for cefamandole.
Oxygen, Compressed USP UN1072 Medical Gas supplied in a) 682 litres and b)165 litres cylinders, Rx only, Oklahoma Respiratory Care 800.262.9857, Norman, OK 73071
Failed impurities/degradation specifications: Purity readings for oxygen were out of specification.
Radiohead Access Point 1.4 GHz Radiohead Access Point  Firmware versions: C.00.04 & C.00.05    Part Number: 989803171211    Product Usage:  IntelliVue Smart-hopping 1.4 GHz Access Point provides wireless connectivity between IntelliVue devices (listed below) and the Philips IntelliVue Information Center. MX40 Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals. The MX4O is to be used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network.
Serial numbers ranging from: US12700465 to US20823366
IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected signal loss of several minutes impacting wireless connectivity
LA MER the spf 18 fluid tint , broad spectrum spf 18, 1.7 fl.oz. liq./50 ml, Shade LIGHT 02, UPC 7 47930 00481 3,  MAX HUBER RESEARCH LABS INC., DIST. NEW YORK, N.Y. 10022 -- MADE IN BELGIUM
all lots currently in the market shipped before June 2013
Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may be subpotent and sunscreen effectiveness may be less than labeled
LA MER the spf 18 fluid tint , broad spectrum spf 18, 1.7 fl.oz. liq./50 ml, Shade MEDIUM 03, UPC 7 47930 00482 0 --- MAX HUBER RESEARCH LABS INC., DIST. NEW YORK, N.Y. 10022 -- MADE IN BELGIUM
LA MER the spf 18 fluid tint , broad spectrum spf 18, 1.7 fl.oz. liq./50 ml, Shade DARK 04, UPC 7 47930 00483 7 --- MAX HUBER RESEARCH LABS INC., DIST. NEW YORK, N.Y. 10022 -- MADE IN BELGIUM
Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may be subpotent and sunscreen effectiveness may be less than labeled
Worldwide Distribution - USA including South Carolina and internationally to Canada and Great Britian.
Spacelabs ARKON Anesthesia Workstation.    Spacelabs ARKON Anesthesia Workstation may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer.
Spacelabs ARKON Anesthesia System is recalled due to software defect.  The System Status Computer may incorrectly determine that a communication error has occurred. If this situation occurs, a buzzer will activate and a yellow triangle will be displayed on the System Status Computer screen that alerts the user of this error.
TEG 5000 Thromboelastograph Coagulation Analyzer   Product Usage:  Multipurpose System for In Vitro Coagulation Studies
Research Use Only (RUO) parameters were included in TEG 5000 User Manual.
White plastic bottle with blue cap containing 90 capsules; Ashwagandha Extract; 450 mg; CODE 4603; Manufactured by NOW FOODS; 395 S. Glen Ellyn Rd., Bloomingdale, IL 60108, USA
It has been determined that this product contains an undeclared ingredient, licorice extract, which contains glycyrrhizin derived from licorice root.
ARTIS zee and zeego x-ray, angiographic system with Software Artis VC20x/VC21A that have Patch 7 and a 3D and DSA license installed.   Angiographic x-ray system
Siemens issued a customer safety advisory notice and field safety corrective action for a potential issue on Artis systems with Artis VC20x/VC21A that have Patch 7 and a 3D and DSA license installed. The issue affects-DSA rotational acquisition. The restriction is related to any rotational 3D-acquisition program with real-time subtraction (e.g. 3D DSA). During the fill phase of the rotational aquisition, the subtraction is not correctly displayed on the live monitor in the control room. As subtracted images are not displayed correctly, this may lead the user to abort or redo the 3D protocol, potentially resulting in the application of an additional dose or contrast agent. 3D data are saved however, and available on the system.
International Distribution including Austria, China, and Germany.
Stryker brand Neuroform 3 Microdelivery Stent System, 4.5 mm X 20 mm, REF Catalog Number: E345020, Model/Product Number: M003450200, Product is manufactured by Boston Scientific Corporation, Fremont, CA and distributed by Stryker Neurovascular, Fremont, CA    The Neuroform Microdelivery Stent System is intended for use with embolic coils for the treatment of wide neck, intracranial, saccular aneurysms arising from a parent vessel with a diameter of greater than equal to 2 mm and greater than equal to 4.5 mm that are not amenable to treatment with surgical clipping.
The device is labeled incorrectly, in that, the device Model Number on the outer carton and inner pouch labels did not match, although both referenced the same lot number. The Model Number on the outer box states UPN M003E345020 (4.5mm x 20 mm Neuroform 3 Stent) while the pouch label states UPN M003E3450300 (4.5mm x 30 mm Neuroform 3 Stent).
C. Pacific Foods is recalling canned mushroom sliced because it contains pesticide levels that are not approved for canned mushroom.
Worldwide Distribution - USA including AL, CA, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NJ, NM, NV, OK, PA, TN, TX, UT, VA & WA. Internationally to Czech Republic, Italy, Japan, Korea & Singapore.
Rultract Retractor Ratchet Cover Plate Distributed by Pemco, Inc., Cleveland, OH 44131   Surgical retractor used to lift the incision site
The firm became aware of the problem when a ratchet cover plate on a device was returned for repair showed signs of corrosion.
Nationwide Distribution including IL, PA, IN, OH, MI, TN, TX, MN, MO, NJ, KY,and MD.
Sodium Bicarbonate, USP  Provided bulk as raw material - label not applicable according to firm    Dialysis Grade 1.5  Dialysis Grade 2    As an API or excipient in the manufacture of Medical Devices and Drugs
Lots and sizes-   20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK  20015437 SBC DIALYSIS 1.5 GRADE 2500 LB SACK     20015443 SBC DIALYSIS 2 GRADE 50 LB BAG
234 sacks at 2500 lbs. each of Dialysis Grade 1.5 ; 880 bags at 50 lbs. each of Dialysis Grade 2
Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate, USP produced by the Old Fort, OH Sodium Bicarbonate Production facility due to metal and other contamination.
PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS, item #18010, Net Wt. 1 lb (454g), UPC 720056180104; item #15502, Net Wt. 8 oz (226.8g),  UPC 001001155027; Stock No. 189, Net Wt. 2 lb (907g)
Pistachios, which were supplied by ARO and subsequently recalled, have the potential to be contaminated with Salmonella.
PRIESTER'S PECANS brand NUTTY FAVORITES ASST, Stock No. 79, Net Wt 1 lb 10 oz (737g)
PRIESTER'S PECANS brand FANCY ROASTED NUTS, Stock No. 7, Net Wt 12 oz (454g)
Worldwide Distribution-USA and the countries of China, Hong Kong, Brazil, France, Japan, Netherlands, Pakistan, Malaysia, United Kingdom, South Korea, Thailand, Dubai, and South Africa.
PASCAL and PASCAL Streamline (532 nm.577 nm);   Treats the patient's eye.
When using the ''Favorites'' function for saved settings, there is potential for a mismatch between displayed power and the actual power output. This may result in over or under treatment.
US Distribution including the states of NV and  MI
ProSpace Peek Implant 5 degree x 8.5 x 22 mm    The device is intended for vertebral body replacement or intervertebral body fusion to aid in the surgical correction or stabilization of the spine. The Aesculap PEEK Spinal Implant System is indicated for use in the thoracolumbar spine (T1 to L5) for partial or total replacement of a collapsed, damaged, or unstable vertebral body due to tumor or trauma to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body.
Aesculap Implant Systems, LLC initiated a recall of the Aesculap Prospace PEEK 5 degree Implant - 8 x 8.5 x 22 mm (SN038P) because the device is incorrectly etched with an 8 degree lordosis instead of a 5 degree lordosis. The device is labeled correctly, only the etching of the implant may be incorrect.
Dried Oregano, cut and sifted; Organic; Product of Turkey,   sold in 25 lb boxes    High Quality Organics, Reno, NV
High Quality Organics was notified by a customer who received a lot of oregano in October 2012, recently tested last box of the shipment and found to be positive for Salmonella.
Pistachios, Salted in the Shell packaged in the following configurations:  1.  Gurley's Golden Recipe Natural Pistachios in 2 oz., 2.25 oz., 12 oz., 3 lb., and 25 lb;  2.  Mountain Country Natural Pistachios, in 2. 25 oz., and 3.5 oz.;  3.  Rachael's Natural Pistachios in 2 oz.
Best by dates between 02-26-14 to 06-03-14
One of our vendors, ARO Pistachio Inc., is issuing an FDA Class 2 Voluntary Recall on certain shipments of pistachios.
Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-4888-20.
Lot #: 15-058-DK*, Exp 1MAR2014; note the * may be followed by 01
Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial.
Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg, packaged in a)100-count bottle (NDC 0591-0737-01), b) 500-count bottle (NDC 0591-0737-05), Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA92880.
Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500 mg are being recalled due to low out of specification (OOS) assay result obtained at expiry (24 months) for the oxycodone portion of the product.
ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse, 0.07%, mint, 33.8 FL OZ (1 L) bottle, Distributed By The Kroger Co., Cincinnati, OH 45202, UPC  0 41260 33606 5.
Microbial Contamination of Non-Sterile Products: This product is being recalled because a stability sample was found to be contaminated with Burkholderia contaminans.