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

23351–23375 of 39702

SevereFDA (Devices)·Z-2537-2016·2016-08-31
Cook Inc. Recalls Roadrunner Uniglide Hydrophilic Wire Guides Due to Glass Contamination
Cook Inc. is recalling Roadrunner Uniglide Hydrophilic Wire Guides because they may be contaminated with glass particles. The recall covers 8,750 devices distributed worldwide.
Product
Roadrunner Uniglide Hydrophilic Wire Guide, Catalog Numbers and GPN: HPWA-18-260, G30489; HPWA-18-320, G30490; HPWA-25-260, G30491; HPWA-35-260, G30492; HPWAS-35-260, G30506; HPW-35-150, G56149; HPW-35-180, G56150; HPWS-35-150, G56152; HPWS-35-180, G56153; HPWA-35-80, G56172…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2357-2016·2016-08-31
Alere INRatio2 PT/INR Testing System Recalled for Inaccurate INR Results
Alere San Diego is voluntarily recalling INRatio2 PT/INR Testing Systems because some patients showed significantly higher INR results in central laboratories than on the device.
Product
Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431 Product 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…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2621-2016·2016-08-31
Cook Inc. Recalls Selective Salpingography Catheters Due to Tip Fracture Risk
Cook Inc. is recalling 7,819 Selective Salpingography Catheters with Beacon Tip due to polymer degradation that can cause the catheter tip to fracture or separate.
Product
Selective Salpingography Catheter with Beacon Tip Cannula, Manipulator/ Injector, Uterine Used for injection of contrast medium into the fallopian tube(s) for selective salpingography.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2661-2016·2016-08-31
Tecan INFINITE F50 Absorbance Reader Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling 19 INFINITE F50 absorbance readers because the batteries may overheat, melt, or char.
Product
SUNRISE 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 obtain…
Category
Medical Device
Distribution
19 states
SevereFDA (Food)·F-1982-2016·2016-08-31
SM Fish Corp. Recalls Dublin Herring for Listeria Risk
SM Fish Corp. is recalling Ossie's Dublin Herring due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
OSSIE'S DUBLIN HERRING, NET WT. 7 OZ., UPC 739885109002; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1951-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling canned black cod, salmon, sardines, steelhead, sturgeon, tuna, and razor clams with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Pacific Black Cod, NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-1463-2016·2016-08-31
Talon Compounding Pharmacy Recalls Sermorelin Injections Due to Sterility Concerns
Talon Compounding Pharmacy is recalling Sermorelin and Sermorelin/GHRP-2 injections because the FDA cannot assure the products are sterile.
Product
Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection, 12 mg, 10 ml depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2664-2016·2016-08-31
Tecan Infinite M1000 Microplate Reader Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling the Infinite M1000 microplate reader because its batteries may overheat, melt, or char.
Product
Tecan Infinite M1000 The Tecan Infinite M1000 is a multifunctional monochromator based microplate reader that provides high performance for the vast majority of todays microplate applications and research. Besides offering absorbance and fluorescence intensity measurements, the…
Category
Medical Device
Distribution
19 states
SevereFDA (Food)·F-1971-2016·2016-08-31
Eatin' Alive Recalls Thai Peanut Noodles for Undeclared Soy Allergen
Paige Common is recalling 24 units of Eatin' Alive Thai Peanut Noodles sold in Oregon due to undeclared soy.
Product
Eatin' Alive VEGAN GLUTEN FREE RAW thai peanut noodles. Keep Refrigerated. 8oz UPC 0 91037 56624 9
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1953-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Wild Columbia River Coho Salmon- Custom Packed, NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1955-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood for Botulism Risk
Northwest Wild Products is recalling various canned seafood products due to potential Clostridium botulinum contamination. Consumers should check for codes starting with OC.
Product
Columbia River Chinook Salmon -Custom Packed, NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1960-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish Due to Botulism Risk
Northwest Wild Products is recalling various canned fish products, including sturgeon, due to potential Clostridium botulinum contamination.
Product
Wild Columbia River Sturgeon - Custom Smoked-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2612-2016·2016-08-31
Cook Inc. Recalls Beacon Tip Catheters Due to Tip Fracture Risk
Cook Inc. is recalling Beacon Tip catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.
Product
Beacon Tip Centimeter Sizing Catheter Beacon Tip White Vessel Sizing Catheter Beacon Tip Vessel Sizing Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1987-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Pickled Herring Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Pickled Herring in 8 oz. plastic tubs because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S PICKLED HERRING, NET WT. 8 OZ., UPC 739885104175; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2618-2016·2016-08-31
Cook Inc. Recalls Liver Access and Biopsy Needle Sets Due to Tip Fracture
Cook Inc. is recalling 52,756 Liver Access and Biopsy Needle Sets because polymer degradation can cause the catheter tip to fracture or separate, potentially leading to device fragments in the body.
Product
Liver Access and Biopsy Needle Set Biopsy needle kit Intended for use in obtaining liver histology samples via a jugular vein approach.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1964-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish Due to Botulism Risk
Northwest Wild Products is recalling canned fish products with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Pacific Black Cod- Custom Smoked -NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1962-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling canned seafood, including razor clams, due to potential Clostridium botulinum contamination. The products were distributed in Oregon via mail order.
Product
Wild Northwest Razor Clams - Custom Smoked-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1984-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Pickled Lox Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Pickled Lox & Cream because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S PICKLED LOX & CREAM, NET WT. 8 OZ., UPC 739885104113; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1957-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Wild Steelhead Salmon - Custom Packed-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2611-2016·2016-08-31
Cook Inc. Recalls Beacon Tip Royal Flush Plus High-Flow Catheters
Cook Inc. is recalling 532,395 Beacon Tip Royal Flush Plus High-Flow Catheters worldwide due to polymer degradation that can cause the catheter tip to fracture or separate.
Product
Beacon Tip Royal Flush Plus High-Flow Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques. Standard techniques for placement of vascular access sheaths…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2662-2016·2016-08-31
Tecan Infinite 200 Absorbance Reader Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling 5 units of the Tecan Infinite 200 absorbance reader because the batteries may overheat, melt, or char.
Product
Tecan Infinite 200. The SUNRISE 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 obtain…
Category
Medical Device
Distribution
19 states
SevereFDA (Food)·F-1963-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products, including razor clams, because they may be contaminated with Clostridium botulinum.
Product
Wild Northwest Razor Clams - Custom Packed-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2617-2016·2016-08-31
Cook Inc. Recalls Kumpe Access Catheters Due to Tip Fracture Risk
Cook Inc. is recalling 26,076 Kumpe Access Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.
Product
Kumpe Access Catheter Cathether, Ureteral, General & Plastic Surgery Used in combination with a HiWire, Bentson, or other flexible-tipped wire guide to gain difficult ureteral access beyond a redundant or tortuous ureteral segment
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1974-2016·2016-08-31
Laxmi Nutkhhata Golden Raisins Recalled for Undeclared Sulfites
House of Spices is recalling Laxmi Nutkhhata Golden Raisins because they contain undeclared sulfites, a major food allergen.
Product
LAXMI NUTKHHAT Golden Raisins, Net Wt. 200g (7 oz), Product of USA -- Distributed by House of Spice Flushing, NY
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-2359-2016·2016-08-31
Alere INRatio 2 Home Monitor Recalled for Inaccurate INR Readings
Alere San Diego is voluntarily recalling INRatio 2 home monitors because they may display inaccurate INR results compared to central laboratory tests.
Product
Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 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 quantitative…
Category
Medical Device
Distribution
Distributed nationwide

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23351–23375 of 39702