Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

23326–23350 of 39702

SevereFDA (Devices)·Z-2358-2016·2016-08-31
Alere INRatio2 PT/INR Home Monitoring System Recalled for Inaccurate INR Results
Alere San Diego is voluntarily recalling INRatio2 PT/INR Home Monitoring Systems because they may display inaccurate INR results compared to central laboratory tests.
Product
Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432, 0200433 Product Usage: Alere INRatio 2 PT/INR Home Monitoring System: The Alere INRatio 2 PT/INR Home Monitoring System, consisting of the INRatio 2 Home Monitor and INRatio PT/INR test strip, is used for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1989-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Pickled Lox Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Pickled Lox because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S PICKLED LOX, NET WT. 8 OZ., UPC 739885104137; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1980-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Wasabi Herring Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Wasabi Herring because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S WASABI HERRING, NET WT. 7 OZ., UPC 739885109088; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2614-2016·2016-08-31
Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Fracture
Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.
Product
Slip-Cath Beacon Tip Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2597-2016·2016-08-31
Conmed Pediatric ThermoGard Electrodes Recalled for Burn Risk
Conmed is recalling Pediatric ThermoGard Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, posing a risk of undetected pad lift and potential burns.
Product
Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.), 10' (3.05m) Cable, Catalog Number 51-7710. Intended to be used for the dispersion and return to the electrosurgical generator.
Category
Medical Device
Distribution
45 states
SevereFDA (Devices)·Z-2651-2016·2016-08-31
Medtronic Evera ICDs Recalled for Rapid Battery Depletion Risk
Medtronic is recalling 78 Evera ICDs and Viva CRT-Ds due to a circuit defect causing rapid battery depletion. Seven confirmed failures have resulted in complications like shortness of breath.
Product
Medtronic, Evera Implantable Cardioverter Defibrillators: Product Model EVERA XT DDBB1D1, DDBB1D4, DDBB2D1, DDBB2D4, DVBB2D4, DVBB1D1. EVERA S DDBC3D1, DDBC3D4 Product Usage: The Medtronic Evera DR dual chamber and Evera VR single chamber, implantable…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1977-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Herring in Sourcream Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Herring in Sourcream because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S HERRING IN SOURCREAM, NET WT. 8 OZ., UPC 739885114174; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2356-2016·2016-08-31
Alere INRatio PT Monitoring Systems Recalled for Inaccurate INR Results
Alere San Diego is voluntarily recalling INRatio PT Monitoring Systems because they may show lower INR results than central laboratory tests, potentially affecting warfarin therapy.
Product
Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio 2 PT Monitoring system is used for the quantitative measurement of Prothrombin Time (PT) in fresh, capillary whole blood. The INRatio 2 PT Monitoring system is intended for use outside the body (in…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1988-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Pickled Herring Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Pickled Herring Clear due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
OSSIE'S PICKLED HERRING CLEAR, NET WT. 8 OZ., UPC 739885104205; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-1468-2016·2016-08-31
Mylan Amlodipine Tablets Recalled for CGMP Deviations
Mylan Institutional is recalling Amlodipine Besylate Tablets 10 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.
Product
Amlodipine Besylate Tablets, USP, 10 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-452-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-452-56; and c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-452-19…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1956-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish Due to Botulism Risk
Northwest Wild Products is recalling various canned fish products because they may be contaminated with Clostridium botulinum.
Product
Wild Steelhead Salmon - Custom Smoked-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1958-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products, including sardines, due to potential Clostridium botulinum contamination.
Product
Oregon Sardines - Mustard-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1972-2016·2016-08-31
Eatin' Alive Recalls Thai Wrap and Noodles for Undeclared Soy
Paige Common dba Eatin' Alive is recalling Thai Peanut Noodles and Thai Wrap because they contain undeclared soy.
Product
Eatin' Alive VEGAN GLUTEN FREE RAW thai wrap. Keep Refrigerated. 6oz UPC 0 91037 56620
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2623-2016·2016-08-31
Cook Inc. Recalls White Lumax Guiding Coaxial Catheters Due to Tip Fracture
Cook Inc. is recalling 3,425 White Lumax Guiding Coaxial Catheters worldwide due to polymer degradation that can cause the catheter tip to fracture or separate.
Product
White Lumax Guiding Coaxial Catheter Catheter, Percutaneous Intended for the delivery of angioplasty balloons and other types of interventional devices.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2616-2016·2016-08-31
Cook Inc. Recalls Haskal Transjugular Intrahepatic Portal Access Sets
Cook Inc. is recalling Haskal Transjugular Intrahepatic Portal Access Sets due to polymer degradation that can cause catheter tip fracture and separation.
Product
Haskal Transjugular Intrahepatic Portal Access Set Introducer, catheter Intended for transjugular liver access in diagnostic and interventional procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2666-2016·2016-08-31
Tecan Hydroflex ELISA Plate Washer Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling Hydroflex ELISA plate washers because the batteries may overheat, melt, or char.
Product
Hydroflex ELISA The HYDROFLEX is a plate washer for 96-well microplates. The instrument is intended to be used primarily in in-vitro diagnostic processing of samples from the human body to obtain information on physiological and pathological states. Software and instrument have…
Category
Medical Device
Distribution
19 states
SevereFDA (Drugs)·D-1466-2016·2016-08-31
Mylan Amlodipine Tablets Recalled for CGMP Deviations
Mylan Institutional, Inc. is recalling Amlodipine Besylate Tablets because they were not manufactured according to Good Manufacturing Practices.
Product
Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1979-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Stiglitz Herring Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Stiglitz Herring in New York and New Jersey because the manufacturing plant tested positive for Listeria monocytogenes.
Product
OSSIE'S STIGLITZ HERRING, NET WT. 7 OZ., UPC 739885109064; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1952-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish Due to Botulism Risk
Northwest Wild Products is recalling various canned fish products with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Wild Columbia River Coho Salmon- Custom Smoked, NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2610-2016·2016-08-31
Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters Due to Tip Fracture
Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.
Product
Beacon Tip Torcon NB Advantage Catheter Catheter, Intravascular, Diagnostic
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2613-2016·2016-08-31
Cook Inc. Recalls Shuttle Select Slip-Cath Catheters Due to Tip Fracture
Cook Inc. is recalling 60,302 Shuttle Select Slip-Cath catheters worldwide due to polymer degradation causing tip fracture and separation.
Product
Shuttle Select Slip-Cath Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2620-2016·2016-08-31
Cook Inc. Recalls Aprima Access Nonvascular Introducer Sets Due to Tip Fracture
Cook Inc. is recalling Aprima Access Nonvascular Introducer Sets because polymer degradation can cause the catheter tip to fracture or separate, potentially leading to medical complications.
Product
Aprima Access Nonvascular Introducer Set Accessories, Catheter Intended for single-puncture percutaneous access to facilitate placement of an .038 inch (0.97 mm) diameter working wire guide for interventional radiology procedures
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2660-2016·2016-08-31
Tecan Infinite F50 Absorbance Reader Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling Infinite F50 absorbance readers because the batteries may overheat, melt, or char.
Product
Infinite F50 instrument. The INFINITE F50 instrument is a 96-well absorbance reader for the measurement of light absorbance (optical density) of liquid media. The instrument is intended to be used primarily in in-vitro diagnostic analysis of samples from the human body to…
Category
Medical Device
Distribution
19 states
SevereFDA (Devices)·Z-2649-2016·2016-08-31
Bovie Precise 360 Handpiece Recalled Due to Incomplete Tip Bond
Bovie Medical Corporation is recalling 95 units of the BVX-450NR Bovie Precise 360 Handpiece because the adhesive bond to the angled tip may be incomplete.
Product
BVX-450NR Bovie Precise 360 Handpiece 45cm, needle Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2650-2016·2016-08-31
Medtronic Recalls 78 Viva Quadripolar Implantable Cardioverter Defibrillators
Medtronic is recalling 78 Viva Quadripolar Implantable Cardioverter Defibrillators because a circuit defect may cause rapid battery depletion. Seven confirmed failures have been reported.
Product
Medtronic, Viva Quadripolar Implantable Cardioverter Defibrillators: Product Model VIVAXTCRT-D DTBA1D1, DTBA1D4 VIVASCRT-D DTBB1D1, DTBB1D4 Product Usage: The Medtronic Viva CRT -D dual chamber, implantable cardioverter defibrillator with cardiac…
Category
Medical Device
Distribution
Distributed nationwide

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23326–23350 of 39702