The Recall Desk

Archive

January 2013 recalls

322 recalls were announced in January 2013.

What the numbers show

Critical
24
Severe
82
High
140
Moderate
51
Low
25

Of the 322 recalls this month scored against our rubric, 7% are Critical, 25% are Severe.

1–100 of 322

  • SevereCPSC·13112·2013-01-31

    SCS Direct Recalls Magnet Balls Due to Ingestion and Injury Risk

    SCS Direct is recalling Magnet Balls sets sold on Amazon.com because swallowed magnets can cause serious intestinal injuries.

    Product
    Magnet Balls® Manipulative Magnet Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13111·2013-01-31

    Kringle Toys Recalls Nanospheres Magnetic Desk Toys Due to Ingestion Hazard

    Kringle Toys and Gifts is recalling Nanospheres Magnetic Desk Toys because swallowed magnets can cause serious internal injuries. The products were sold exclusively on Amazon.com.

    Product
    Nanospheres Magnetic Desk Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13113·2013-01-31

    World Imports Recalls Bunk Beds Due to Safety Standard Violation

    World Imports is recalling specific bunk bed models because the openings between metal rails violate safety standards, posing a risk of entrapment or asphyxiation.

    Product
    Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13110·2013-01-31

    MegaFood One Daily Supplement Bottles Recalled for Non-Child-Resistant Packaging

    FoodState Inc. is recalling MegaFood One Daily Supplement bottles because they lack required child-resistant packaging. The tablets contain iron, which poses a serious risk to young children.

    Product
    MegaFood One Daily Supplement Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0932-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 951 lbs of H E B brand cold smoke salmon due to potential Listeria monocytogenes contamination.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***H E B***ALL NATURAL***SMOKED***SALMON***Sliced and Ready to Serve***4 oz***
    Category
    Food
    Distribution
    17 states
  • CriticalCPSC·13105·2013-01-30

    Natart Chelsea Dressers Recalled Due to Tip-Over Hazard and Reported Death

    Gemme Juvenile is recalling Natart Chelsea Dressers because a toddler reportedly suffocated after the unit tipped over. Consumers should stop using the dressers and obtain free wall anchor kits.

    Product
    Natart Chelsea Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0930-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 1,080 lbs of Royal Fjord Smoked Salmon Toppers due to potential Listeria monocytogenes contamination.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***Royal Fjord*** Smoked Salmon***Toppers***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0925-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA, LLC is recalling 4,800 lbs of Cold Smoke Salmon due to potential Listeria monocytogenes contamination. The product was distributed across 16 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***BLACK BEAR***of the BLACK FOREST*** Naturally Smoked***Smoked Salmon***Extra Fancy***1 lb.***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0929-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 800 lbs of cold smoke salmon due to potential Listeria monocytogenes contamination. The product was distributed across 16 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***Silver***Source***Smoked***Salmon***Salmon Salar***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0934-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling Cold Smoke Salmon in vacuum plastic bags due to potential contamination with Listeria monocytogenes.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***Smoke***Nova***Salmon***Supreme Fine Foods*** 2lb***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0935-2013·2013-01-30

    Marine Harvest USA Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling cold smoke salmon products due to a potential contamination with Listeria monocytogenes. The affected products were distributed across 17 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***New England Smoked Salmon***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0933-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon Due to Listeria Risk

    Marine Harvest USA is recalling Royal Fjord Smoked Salmon Rounds due to potential Listeria monocytogenes contamination. The product was distributed in 16 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***Royal Fjord***Smoked Salmon***Rounds***5oz***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-0928-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling cold smoked salmon due to potential Listeria monocytogenes contamination. The product was distributed across 17 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags. Food Service Whole Smoked Side. Labeled in part: ***Unsliced Cold Smoked*** Salmon Fillet Skin On***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Devices)·Z-0706-2013·2013-01-30

    DePuy Spine Recalls VIPER Polyaxial Screws Due to Potential Separation

    DePuy Spine is recalling 36 units of VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Code: 1867-15-880 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0705-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screw Recall for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0922-2013·2013-01-30

    Haig's Delicacies Recalls Tyropita Pastries Due to Undeclared Allergens

    Haig's Delicacies is recalling Tyropita pastries because they contain undeclared wheat, milk, and eggs. The products were distributed in California, Washington, and Maryland.

    Product
    Tyropita; a triangular phyllo dough pastry with cheese filling. sold in 5 lb. bulk Foodservice cases . Undeclared wheat, milk and eggs. Manufactured by Haig s Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0919-2013·2013-01-30

    Haig's Delicacies Recalls Tzatziki for Undeclared Milk Allergen

    Haig's Delicacies is recalling Tzatziki yogurt products sold in California, Washington, and Maryland because they contain undeclared milk, wheat, and eggs.

    Product
    Tzatziki; Greek yogurt with cucumber and dill. sold in 8 oz retail and 5 lb bulk food service containers. Undeclared milk. Manufactured by Haigs Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0709-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws 8x80mm and larger because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Product Code: 1867-15-980 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-135-2013·2013-01-30

    Genentech Recalls Trastuzumab Kits Due to Potential Glass Particulates

    Genentech is recalling 2,140 Trastuzumab Kits for investigational use because the included Bacteriostatic Water for Injection diluent vials may contain glass particulates.

    Product
    Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg); 1 20 mL multiple dose vial Bacteriostatic Water for Injection, USP (1.1% benzyl alcohol), Manufactured by Hospira, Inc., for Genentech, Inc., South San Francisco, CA 94080-4990, NDC 50242-903-69; and 1 Reco
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·13107·2013-01-30

    Sportspower BouncePro 14' Trampolines Recalled for Fall Hazard

    Sportspower is expanding a recall of BouncePro 14' trampolines sold at Walmart because the enclosure netting can break, posing a fall hazard.

    Product
    Sportspower BouncePro 14' Trampolines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0710-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER polyaxial screws because the shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Code: 1867-15-999 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-130-2013·2013-01-30

    West-ward Recalls Lisinopril Tablets Due to Foreign Substance Presence

    West-ward Pharmaceutical Corp. is recalling specific lots of Lisinopril Tablets, USP 40 mg, because uncharacteristic black spots were found in the tablets.

    Product
    Lisinopril Tablets, USP 40 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1270-01); b) 1000-count tablets per bottle (NDC 0143-1270-10); Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724; and c) 1000-count tablets per bottle (NDC 24658-245-
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0711-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Disassociation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Product Code: 1867-15-170 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0931-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 4,572 lbs of Cold Smoke Salmon due to potential Listeria monocytogenes contamination.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***SMOKED***SALMON***Deli Sliced***Ready to Serve***Royal Fjord***Center***Cut Loin***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Devices)·Z-0707-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Code: 1867-15-899 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0713-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Component Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: 1867-15-199 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0712-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Product Code: 1867-15-180 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-131-2013·2013-01-30

    West-ward Recalls Propylthiouracil Tablets Due to Foreign Substance Presence

    West-ward Pharmaceutical Corp. is recalling specific lots of Propylthiouracil Tablets, USP, 50 mg because uncharacteristic spots identified as steel corrosion, degraded tablet material, and hydrocarbon oil were found.

    Product
    Propylthiouracil Tablets, USP, 50 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1480-01) and b) 1000-count tablets per bottle (NDC 0143-1480-10), Rx only, Manufactured by: West-ward Pharmaceuticals Corp. Eatontown, NJ 07724.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0708-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screw Recall for Potential Disassociation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Code: 1867-15-970 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-132-2013·2013-01-30

    West-ward Recalls Lisinopril and Hydrochlorothiazide Tablets Due to Foreign Particulates

    West-ward Pharmaceutical Corp. is recalling specific lots of Lisinopril and Hydrochlorothiazide Tablets because they contain minute stainless steel particulates.

    Product
    Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0915-2013·2013-01-30

    Wegmans Recalls Organic Spinach and Spring Mix Due to E. coli Risk

    Wegmans is recalling 5 oz and 11 oz packages of Organic Spinach and Spring Mix Blend because the product may be contaminated with E. coli O157:H7.

    Product
    Wegmans Organic Spinach & Spring Mix --- Product is packaged in clam shell in two sizes: 5oz and 11oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0926-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling 1 lb. vacuum-packed cold smoked salmon potentially contaminated with Listeria monocytogenes.

    Product
    Cold Smoke Salmon in vacuum plastic bags. Food Service Cold Smoked Salmon Trim 1 lb.
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-0724-2013·2013-01-30

    ConMed Recalls ABC Nozzles Due to Compromised Sterile Pouch Seals

    ConMed is recalling 313,190 ABC Nozzles because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catalog No. 130343, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0729-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode, 1 inch Coated Blade, REF/Catalog No. 139100, Single Use, Sterile, Rx ONLY --CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V030000·2013-01-30

    Lexus IS Models Recalled for Potential Wiper Arm Failure

    Toyota is recalling specific Lexus IS models because wiper arm nuts may be insufficiently torqued, potentially causing wipers to stop working.

    Product
    LEXUS — LEXUS IS 350C, IS F, IS 250, IS 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0730-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 1 inch Coated Needle, REF/Catalog No. 139102, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0721-2013·2013-01-30

    ConMed Recalls Goldvac UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling Goldvac UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catalog No. 60-7523-001, Sterile, Rx ONLY -- CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 6 inch Coated Needle with Extended Insulation, REF/Catalog No. 139108, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0923-2013·2013-01-30

    Pepsi Wild Cherry Recall Due to Swapped Labels for Phenylketonuria Risk

    Pepsi Cola North America is recalling two-liter bottles of Diet Wild Cherry Pepsi because labels were swapped with Regular Pepsi, posing a risk to individuals with phenylketonuria or diabetes.

    Product
    Diet Wild Cherry Pepsi two liter plastic bottles UPC 1234107
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0921-2013·2013-01-30

    Haig's Delicacies Recalls Spanakopita for Undeclared Allergens

    Haig's Delicacies is recalling Spanakopita pastries sold in 5 lb. bulk cases because they contain undeclared wheat, milk, and eggs.

    Product
    Spanakopita; a triangular phyllo dough pastry with spinach and cheese filling. sold in 5 lb. bulk Foodservice cases. Undeclared wheat, milk and eggs Manufactured by Haig's Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0722-2013·2013-01-30

    ConMed Recalls Goldvac UltraClean Accessory Electrode Due to Compromised Sterile Seals

    ConMed is recalling Goldvac UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 60-7524-001, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2013·2013-01-30

    ConMed Recalls Goldvac UltraClean Electrode Blades Due to Compromised Sterile Seals

    ConMed is recalling Goldvac UltraClean Accessory Electrode Blades because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    Goldvac(TM) UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended Insulation, REF/Catalog No. 60-7521-001, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0927-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling cold smoked salmon products due to potential contamination with Listeria monocytogenes. The recall affects specific lots distributed across multiple states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***HAND-PACKED***DARN GOOD***Atlantic Smoked Salmon***KOSHER***einsteinbros.com***
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-0732-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended Insulation, REF/Catalog No. 139105EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0698-2013·2013-01-30

    Abbott Vitamin D Reagent Kit Recalled for Inaccurate Test Results

    Abbott Laboratories is recalling ARCHITECT 25-OH Vitamin D Reagent Kits because they may produce falsely elevated or depressed results when used with specific Reaction Vessel lots.

    Product
    Abbott Laboratories, ARCHITECT 25-OH Vitamin D Reagent Kit, 03L52-25 (ROW) and 03L52-27 (U.S.) (1 x 100 tests), 03L52-35 (ROW) and 03L52-37 (U.S.) (5 x 100 tests); in vitro diagnostic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0737-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended Insulation, REF/Catalog No. 139112EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0920-2013·2013-01-30

    Haig's Delicacies Recalls Falafel with Tahini Sauce for Undeclared Allergens

    Haig's Delicacies is recalling Falafel with Tahini Sauce because it contains undeclared milk, wheat, and eggs.

    Product
    Falafel with Tahini Sauce; nuggets of ground garbanzo beans with a rich, tangy tahini sauce. Sold in 5 oz retail rectangular deli containers and 5 lb bulk foodservice. Undeclared wheat Manufactured by Haigs Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·13V029000·2013-01-30

    Toyota and Pontiac Recall 2003-2004 Models for Airbag Defect

    Toyota and Pontiac are recalling 2003-2004 Corolla, Corolla Matrix, and Vibe vehicles because airbag circuits may short, causing unintended deployment.

    Product
    PONTIAC — PONTIAC, TOYOTA VIBE, COROLLA, COROLLA MATRIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrode Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 6 inch Coated Blade, REF/Catalog No. 139107, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0918-2013·2013-01-30

    Conagra Recalls Andy Capp's Cheddar Cheese Fries Due to Unlabeled Soy

    Conagra Inc is recalling Andy Capp's Cheddar Cheese Fries because they were packaged in Hot Fries bags that do not list soy as an ingredient.

    Product
    Andy Capp's Cheddar Cheese Fries packaged in Andy Capp's Hot Fries, 0.85-oz foil bags, snack size, Case UPC: 20-0-26200-47169-7 and Unit UPC: 00-0-26200-47168-6.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0725-2013·2013-01-30

    ConMed Recalls TUR Endoscopic Cables Due to Compromised Sterile Pouch Seals

    ConMed is recalling 313,190 TUR/Endoscopic Cables because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    TUR/Endoscopic Cable, 10 feet (3.05 mm), REF/Catalog No. 135171, Disposable, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0736-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrode Blades Due to Seal Compromise

    ConMed is recalling UltraClean Accessory Electrode 4 inch Coated Blades because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 139112, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V028000·2013-01-30

    Entegra Recalls Motorhomes Due to Short Wiper Link Defect

    Entegra Coach is recalling 2011-2013 Aspire, Anthem, and 2012-2013 Cornerstone motorhomes because a short wiper link may reduce driver visibility, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA ASPIRE, CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0728-2013·2013-01-30

    ConMed Recalls Electrosurgical Tip Cleaners Due to Compromised Sterile Seals

    ConMed is recalling 313,190 Electrosurgical Tip Cleaners because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    Electrosurgical Tip Cleaner, REF/Catalog No. 138029, Single Use, Sterile, Rx ONLY -- Distributed By: CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0723-2013·2013-01-30

    ConMed Recalls Goldvac UltraClean Accessory Electrode Due to Seal Compromise

    ConMed is recalling Goldvac UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade, REF/Catalog No. 60-7526-001, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0719-2013·2013-01-30

    ConMed Recalls Disposable Hyfrecator Electrodes Due to Compromised Sterile Seals

    ConMed is recalling 313,190 disposable Hyfrecator electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-101-8CS, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0731-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrode Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended Insulation, REF/Catalog No. 139104EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION 525 Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0715-2013·2013-01-30

    Medisystems 17 Gauge AV Fistula Needles Recalled for Mislabeling

    Medisystems is recalling 17 Gauge AV Fistula Needles because single needle packs are mislabeled as 15 Gauge. The recall covers 4,000 needles distributed in New York, Pennsylvania, and Tennessee.

    Product
    Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB Product Usage: Medisystems AVF with MasterGuard anti-stick needle protector is indicated for use as a vascular access device in hemodialysis or other extracorporeal procedures. It is intended for use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0924-2013·2013-01-30

    Pepsi Wild Cherry Recall Due to Swapped Labels

    Pepsi Cola North America is recalling Regular and Diet Wild Cherry Pepsi two-liter bottles because labels were swapped during production, posing a risk to individuals with phenylketonuria or diabetes.

    Product
    Regular Wild Cherry Pepsi two liter plastic bottles UPC 1231100
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0916-2013·2013-01-30

    Cardinal Health Recalls Dairy Aid Lactase Caplets Due to Labeling Error

    Cardinal Health is recalling specific lots of Dairy Aid Lactase Enzyme Supplement caplets because the packaging incorrectly lists the strength as 9,000 FCC Units instead of 3,000 FCC Units.

    Product
    Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0727-2013·2013-01-30

    ConMed Recalls Electrosurgical ENT Needle Electrodes Due to Compromised Sterile Seals

    ConMed is recalling 313,190 electrosurgical ENT needle electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    ELECTROSURGICAL ENT NEEDLE ELECTRODE, 6 inch with Extended Insulation, REF/Catalog No. 138025, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0699-2013·2013-01-30

    Becton Dickinson Recalls BBL Crystal Enteric/Nonfermenter ID Kits

    Becton Dickinson is recalling BBL Crystal Enteric/Nonfermenter ID Kits because reversed reagent positions may cause bacteria misidentification.

    Product
    Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit, Catalog # 24500, cartons of 20 kits, In-vitro diagnostic reagents for microbiological testing. The BBL Crystal Enteric/Nonfermentor (E/NF) identification (ID) System is for the identification of aerobic gram
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-0696-2013·2013-01-30

    Roche COBAS INTEGRA 400 Analyzer Recalled for Software Security Issue

    Roche is recalling COBAS INTEGRA 400 analyzers due to a security vulnerability in the Oracle TNS-Listener component that could allow unauthorized database access.

    Product
    Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0735-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling 313,190 UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catalog No. 139110EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0716-2013·2013-01-30

    Abbott i-Stat cTnI Cartridges Recalled for Incorrect Barcode

    Abbott Point of Care Canada Limited is recalling 10 boxes of i-Stat cTnI cartridges from lot P12179 due to incorrect barcodes on the cartridge portion pack.

    Product
    Abbott Point of Care i-Stat cTnI cartridge. The i-Stat cardiac troponin I (cTnI) test is an in vitro diagnostic test for the quantitive measurement of cardiac troponin I (cTnI) in whole blood or plasma. Measurements of cardiac troponin I are used in the diagnosis and treatment
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0701-2013·2013-01-30

    BD MAX Clinical Diagnostic Instruments Recalled for Minor Defects

    Becton Dickinson is recalling 86 BD MAX clinical diagnostic instruments because minor defects may cause erroneous test results.

    Product
    Becton, Dickinson and Company, BD MAX (tm) (6 channel) Instruments, Catalog number 441916, clinical diagnostic instrument.
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0717-2013·2013-01-30

    Ansell Recalls Lifestyles Condoms Due to Mislabeling of Ultra Thin Style

    Ansell Healthcare Products LLC is recalling one lot of Lifestyles Pleasure Collection condoms because Ultra Thin condoms were included instead of the labeled Skyn style.

    Product
    Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of Ultra Sensitive, Flavors and Colors, Skyn, Thryll, Thyn, and Ultra Thin. UPC 0-70907-02625-0.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0700-2013·2013-01-30

    AMS GreenLight HPS and XPS Surgical Lasers Recalled for Electrical Non-Conformance

    AMS Innovative Center is recalling 389 GreenLight HPS and XPS surgical laser systems because the Voltage Scaling Board failed to meet IEC 60601-1-2 electrical safety standards.

    Product
    GreenLight HPS (High Performance System) GreenLight XPS (Xcelerated Performance System) Manufactured by AMS, Solutions for Life Innovation Center. GreenLight HPS and XPS Surgical Lasers Systems and accessories are intended for use in endoscopic 532 nm laser resection of t
    Category
    Medical Device
    Distribution
    0 states
  • ModerateNHTSA·13V034000·2013-01-30

    Wilson Livestock Trailer Recall for Lift Deck Guide Failure

    Wilson Trailer Company is recalling 2007-2013 livestock trailers because plastic deck guides may fail, allowing the lift deck to shift and fall.

    Product
    WILSON — WILSON LIVESTOCK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0714-2013·2013-01-30

    Medisystems Buttonhole Needle Set Recalled for Mislabeled Length

    Medisystems is recalling 5 mislabeled buttonhole needle pouches that were labeled as 15 Ga x 1 inch instead of 15 Ga x 3/5 inch.

    Product
    Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Code: BH-2035PE Product Usage: Medisystems Buttonhole Needle Sets are indicated for use as an access device for dialysis and pheresis procedures using a constant site orbuttonhole method of needle insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0718-2013·2013-01-30

    ConMed Recalls Disposable Hyfrecator Electrodes Due to Compromised Sterile Seals

    ConMed is recalling 313,190 disposable Hyfrecator electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP, Disposable Hyfrecator(R) Tips, REF/Catalog No. 7-100-8CS, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-133-2013·2013-01-30

    West-ward Recalls Prednisone Tablets Due to Foreign Substance Presence

    West-ward Pharmaceutical Corp. is recalling PredniSONE Tablets, USP, 20 mg, due to the presence of foreign substances including stainless steel inclusions.

    Product
    PredniSONE Tablets, USP, 20 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1477-01), b) 500-count tablets per bottle (NDC 0143-1477-05), and c) 1000-count tablets per bottle (NDC 0143-1477-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatowntown, NJ 07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0726-2013·2013-01-30

    ConMed Recalls Electrosurgical Safety Holsters Due to Compromised Sterile Seals

    ConMed is recalling 313,190 electrosurgical safety holsters because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    CONMED(R) ELECTROSURGICAL SAFETY HOLSTER, Disposable Safety Holster, REF/Catalog No. 137668, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-134-2013·2013-01-30

    Major Oral Peroxide Recalled Due to Stability Data Concerns

    Axcentria Pharmaceuticals is recalling Major Oral Peroxide because stability data indicates the product degrades below acceptable levels before the printed expiration date.

    Product
    Major Oral Peroxide (Carbamide Peroxide 10%), 2 fl oz (60 mL), Distributed by: Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-4062-03
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Food)·F-0917-2013·2013-01-30

    Coca-Cola Recalls 12-Ounce Cans Due to Off Taste and Odor Complaints

    The Coca-Cola Company is recalling 12-ounce aluminum cans in Florida due to complaints of off taste and odor.

    Product
    Coca-Cola, 12 fluid ounce aluminum cans in 20-packs and 32-packs, The Coca Cola Company.
    Category
    Food
    Distribution
    1 state
  • LowFDA (Drugs)·D-136-2013·2013-01-30

    Flanax Antacid Recalled for Missing Tamper-Evident Cap Band

    Belmora LLC is recalling 17,996 bottles of Flanax antacid because the caps lack a tamper-evident breakaway band.

    Product
    Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·13103·2013-01-29

    BRP Recalls Can-Am Commander Side-by-Side Vehicles Due to Fire Hazard

    BRP is recalling approximately 25,000 Can-Am Commander side-by-side vehicles because accumulated debris in the exhaust pipe area poses a fire risk.

    Product
    Can-Am® Commander Side-by-Side Off Road Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13104·2013-01-29

    Columbia Recalls Seven Heated Jacket Models Due to Burn Hazard

    Columbia Sportswear is recalling seven models of heated jackets because the inner wrist cuffs can overheat, posing a burn risk.

    Product
    Men's and Women's Heated Jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V032000·2013-01-29

    Triumph Recalls 2011-2012 Motorcycles Due to Wheel Bearing Quality Issues

    Triumph is recalling specific 2011-2012 motorcycles because wheel bearings of unknown quality could fail, increasing crash risk. Dealers will replace the bearings free of charge.

    Product
    TRIUMPH — TRIUMPH DAYTONA 675, STREET TRIPLE, THUNDERBIRD, THUNDERBIRD STORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13102·2013-01-25

    Specialized Recalls Tarmac, Crux, and Secteur Bicycles Due to Fork Breakage

    Specialized Bicycle Components is recalling approximately 12,200 Tarmac SL4, Crux, and Secteur bicycles because the front fork steerer tube can break, posing a fall hazard.

    Product
    Specialized Bicycle Components Tarmac SL4 Crux Secteur Road Bicycles and Frame Sets
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V027000·2013-01-25

    PACCAR Recalls 2013 Kenworth and Peterbilt Trucks for Suspension Software Defect

    PACCAR is recalling specific 2013 Kenworth T680 and Peterbilt 567/579 trucks because a software defect may cause the rear air suspension to re-inflate unexpectedly, posing an injury risk.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 567, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V026000·2013-01-24

    Dutchmen Recalls 2007-2011 Recreational Trailers Due to Fire Risk

    Dutchmen is recalling specific 2007-2011 recreational trailers because inadequate wiring in the transfer switch may cause overheating and fire.

    Product
    DUTCHMEN — DUTCHMEN WINNERS CIRCLE, N TENSE, GRAND JUNCTION, MONTE VISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V025000·2013-01-24

    Stoughton AHV Trailers Recalled for Frame Fatigue Cracks

    Stoughton Trailers is recalling 2009-2011 AHV grain haulers because fatigue cracks in the frame structure could lead to vehicle failure and loss of control.

    Product
    STOUGHTON — STOUGHTON AHV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E003000·2013-01-24

    Vision Wheel Recalls Prado Aftermarket Wheels Due to Fracture Risk

    Vision Wheel is recalling certain Prado model aftermarket wheels because they may fracture during normal use, potentially leading to tire failure or loss of vehicle control.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V023000·2013-01-24

    GM Recalls Certain 2012 Vehicles for Driver Air Bag Deployment Risk

    General Motors is recalling certain 2012 Chevrolet Camaro, Cruze and Sonic, and Buick Verano vehicles because a driver air bag may fail to deploy in a crash.

    Product
    BUICK — BUICK, CHEVROLET VERANO, CRUZE, SONIC, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0907-2013·2013-01-23

    Nautifish Frozen Cooked Lobster Meat Recalled for Listeria monocytogenes

    Cap Sur Mer, Inc. is recalling Nautifish Frozen Cooked Lobster Meat because laboratory analysis detected Listeria monocytogenes.

    Product
    Nautifish Frozen Cooked Lobster Meat. CKL 12 X 11.3 oz. Metal Cans. 12 items/case. Keep Frozen.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0913-2013·2013-01-23

    Ocean Beauty Recalls Cold-Smoked Salmon for Listeria Contamination

    Ocean Beauty Seafoods is recalling 3-ounce packages of Nathan's Nova Salmon because a sample tested positive for Listeria monocytogenes.

    Product
    Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink. Nathan's, 3oz Nova Salmon, has the UPC 0 73030 80368 2. The front panel is labeled in part: "***NATHAN'S TRADITIONAL DELICATESSEN NOVA SALMON CLASSIC SMOK
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0914-2013·2013-01-23

    Ocean Beauty Recalls Lascco Smoked Salmon for Listeria Contamination

    Ocean Beauty Seafoods is recalling Lascco brand smoked salmon after samples tested positive for Listeria monocytogenes. The product was distributed nationwide to retailers in 12 states.

    Product
    Cold-smoked salmon in vacuum plastic that are partially clear and partially colored blue, yellow, and white. Lascco, 4 oz Nova Salmon, has the UPC 0 72840 01751 7. The front panel is labeled in parts: "***Lascco BRAND SLICED*** SMOKED NOVA SALMON NET WT 4 OZ (113g) PERIS
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0912-2013·2013-01-23

    Frozen Cooked Lobster Meat Recalled for Listeria monocytogenes Contamination

    Cap Sur Mer, Inc. is recalling frozen cooked lobster meat found to contain Listeria monocytogenes. The product was distributed in New Hampshire and Massachusetts.

    Product
    Frozen Cooked Lobster Meat. TCK Nautifish 6 X 2 lbs. Plastic Bags, 6 individual per case. Keep Frozen
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0908-2013·2013-01-23

    Apollo Frozen Cooked Lobster Meat Recalled for Listeria monocytogenes

    Cap Sur Mer, Inc. is recalling Apollo Frozen Cooked Lobster Meat due to the presence of Listeria monocytogenes detected in laboratory analysis.

    Product
    Apollo Frozen Cooked Lobster Meat. BCKL Lobster Meat 6X2 lb, plastic bags, 6 individual items per case, keep frozen
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0672-2013·2013-01-23

    Bausch and Lomb Amvisc Cannulas Recalled for Detachment Risk

    Bausch and Lomb is recalling Amvisc and Amvisc Plus cannulas that may detach from syringes during injection, posing a risk of serious patient injury.

    Product
    Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081, 59051L, 59081L) and Amvisc Plus 1.6% Sodium Hyaluronate (Model 60081, 60051, 60051L, 60081L) ophthalmic viscosurgical device. The 27G disposable cannula is a
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-0886-2013·2013-01-23

    Woodstock Tamari Almonds Recalled for Undeclared Soy Ingredient

    Woodstock Farms is recalling Tamari Almonds because the label fails to list soy, a major allergen, posing a risk of severe allergic reactions.

    Product
    Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.
    Category
    Food
    Distribution
    26 states
  • SevereNHTSA·13V022000·2013-01-23

    Thomas Built Buses Recalls Saf-T-Liner EFX School Buses for Lighting Defect

    Daimler Trucks North America is recalling 2013-2014 Thomas Built Buses Saf-T-Liner EFX school buses because a circuit breaker may trip, causing a loss of power to headlights and other lights.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0879-2013·2013-01-23

    Somersault Cinnamon Crunch Recalled for Undeclared Milk Allergen

    Somersault Snack Co. is recalling Cinnamon Crunch sunflower seed snacks because the packaging failed to declare a milk allergen present in a flavor ingredient.

    Product
    Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds and toasted grains. Sunflower seed snack. .5 oz, 1 oz., 2 oz., 6 oz., and 16 oz.
    Category
    Food
    Distribution
    Distributed nationwide

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