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

23376–23400 of 39702

SevereFDA (Devices)·Z-2615-2016·2016-08-31
Cook Inc. Recalls FluoroSet Radiographic Tubal Assessment Sets
Cook Inc. is recalling 1,881 FluoroSet Radiographic Tubal Assessment Sets due to polymer degradation that can cause catheter tip fracture or separation.
Product
FluoroSet Radiographic Tubal Assessment Set Cannula, Manipulator/ Injector, Uterine Used for instillation of contrast media into the uterine cavity for radiographic evaluation of the uterine cavity and for injection of appropriate contrast media into the fallopian tubes for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2663-2016·2016-08-31
Tecan Infinite 200 PRO Microplate Reader Recalled for Battery Overheating
Tecan US, Inc. is recalling 27 Infinite 200 PRO microplate readers because the batteries may overheat, melt, or char.
Product
Infinite 200 PRO The Tecan Infinite 200 PRO is a multifunctional microplate reader with injector option. The Infinite 200 PRO provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The Infinite 200 PRO has been…
Category
Medical Device
Distribution
19 states
SevereFDA (Devices)·Z-2361-2016·2016-08-31
Alere INRatio PT/INR Test Strips Recalled for Inaccurate INR Readings
Alere San Diego is voluntarily recalling INRatio PT/INR test strips and meters because they may display therapeutic INR values that are significantly higher in central laboratory testing.
Product
Alere INRatio PT/INR Test Strips Model Number: 0100071, 0100139 Product Usage: The INRatio/INRatio2 Test Strips perform a modified version of the one-stage Prothrombin Time test, using a recombinant human thromboplastin reagent. The clot formed in the Prothrombin Time…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1976-2016·2016-08-31
SM Fish Corp. Recalls Ossie's Pickled Lox Due to Listeria Risk
SM Fish Corp. is recalling Ossie's Pickled Lox Dairy because the manufacturing plant tested positive for Listeria monocytogenes. The product was distributed in New York and New Jersey.
Product
OSSIE'S PICKLED LOX DAIRY, NET WT. 8 OZ., UPC 739885114136; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1966-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products, including tuna, salmon, and black cod, due to potential Clostridium botulinum contamination.
Product
Pacific White Albacore Tuna - Custom Packed -NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2355-2016·2016-08-31
Alere INRatio PT/INR Monitoring Systems Recalled for Inaccurate INR Results
Alere San Diego is voluntarily recalling INRatio PT/INR Monitoring Systems because they may report inaccurate INR values, potentially leading to incorrect anticoagulant dosing.
Product
INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007 Product Usage: The INRatio Prothrombin Time Monitoring System uses a modified version of the one-stage PT test. After a drop of blood is applied to the test strip, it is drawn into the test area and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1983-2016·2016-08-31
SM Fish Corp. Recalls Honey Mustard Herring for Listeria Risk
SM Fish Corp. is recalling 336 containers of Ossie's Honey Mustard Herring due to potential Listeria monocytogenes contamination. The product was distributed in New York and New Jersey.
Product
OSSIE'S HONEY MUSTARD HERRING; NET WT. 7 OZ. 739885109019; -- Far Rockaway, NY 11691 --- The product is packed in a plastic deli tub.
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-2665-2016·2016-08-31
Tecan Infinite M1000 PRO Microplate Reader Recalled for Battery Overheating Risk
Tecan US, Inc. is recalling 11 Infinite M1000 PRO microplate readers because their batteries may overheat, melt, or char.
Product
Tecan Infinite M1000 PRO The Tecan Infinite M1000 PRO is a multifunctional monochromator-based microplate reader that provides high performance for the vast majority of todays microplate applications and research. In addition to offering absorbance and fluorescence intensity…
Category
Medical Device
Distribution
19 states
SevereFDA (Food)·F-1961-2016·2016-08-31
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 can codes and stop using affected items.
Product
Pacific White Albacore Tuna - Custom Smoked -NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2596-2016·2016-08-31
Conmed Dual Dispersive Electrodes Recalled for Burn Risk
Conmed is recalling Adult ThermoGard Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, posing a risk of undetected pad lift and potential burns.
Product
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), No Cable, Catalog Number 51-7410. Intended to be used for the dispersion and return to the electrosurgical generator.
Category
Medical Device
Distribution
45 states
SevereFDA (Devices)·Z-2354-2016·2016-08-31
Alere INRatio PT/INR System Recalled for Inaccurate Warfarin Monitoring Results
Alere San Diego is voluntarily recalling INRatio PT/INR Monitoring Systems because they may show lower INR values than central laboratory tests, potentially affecting warfarin dosing.
Product
Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product Usage: Alere INRatio ¿ 2 PT/INR Monitoring System (Professional Use): The Alere INRatio ¿ 2 PT/INR Monitoring System (Professional Use), consisting of the INRatio ¿ 2 Monitor and INRatio¿ 2 PT/INR test…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2622-2016·2016-08-31
Cook Inc. Recalls Transluminal Biliary Biopsy Forceps Sets Due to Tip Fracture
Cook Inc. is recalling 2,606 Transluminal Biliary Biopsy Forceps Sets because polymer degradation can cause the catheter tip to fracture or separate, potentially leading to device fragments in the body.
Product
Transluminal Biliary Biopsy Forceps Set Forceps, Biopsy, Non-Electric Intended for access to and biopsy of tissue within the biliary ductal system
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2609-2016·2016-08-31
Baxter HomeChoice Peritoneal Dialysis Systems Recalled for Software Defect
Baxter is recalling HomeChoice and HomeChoice PRO automated peritoneal dialysis systems due to a software defect that may cause serious complications in patients with ascites.
Product
1) The HomeChoice automated peritoneal dialysis system. Dataplate located on the device is labeled in part: Baxter. 2) The HomeChoice PRO automated peritoneal dialysis system. Dataplate located on the device is labeled in part: Baxter. The HomeChoice/HomeChoice Pro…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2360-2016·2016-08-31
Alere INRatio2 PT/INR Monitoring System Recalled for Inaccurate INR Results
Alere San Diego is voluntarily recalling INRatio2 PT/INR Monitoring Systems because they may report inaccurate INR results, potentially leading to incorrect anticoagulant dosing.
Product
Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A Product Usage: The Alere INRatio¿/INRatio¿2 system uses a modified version of the one-stage PT test. After a drop of blood is applied to the test strip, it is drawn into the test area and mixed with…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V634000·2016-08-31
Daimler Trucks Recalls 2014-2017 Models Due to Front Axle Hub Failure Risk
Daimler Trucks North America is recalling specific 2014-2017 Freightliner and Western Star trucks because front axle hubs may fail, causing the wheel to separate from the axle.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER 4800, 5700, 108SD, CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2362-2016·2016-08-31
Alere INRatio PT/INR Test Strips Recalled for Inaccurate Results
Alere San Diego is voluntarily recalling INRatio test strips because they may report inaccurate INR results, potentially affecting warfarin therapy.
Product
Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU, 99007G1, 99007G3, 99007G5, 99007G7, 99008EU, 99008G1, 99008G3, 99008G5, 99008G7 Product Usage: The Alere INRatio¿/INRatio¿2 system uses a modified version of the one-stage PT test. After a drop of blood is…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2619-2016·2016-08-31
Cook Inc. Recalls Neff DAgostino Percutaneous Access Sets Due to Tip Fracture
Cook Inc. is recalling 5,020 Neff DAgostino Percutaneous Access Sets because polymer degradation can cause the catheter tip to fracture or separate, potentially leading to device fragments in the body.
Product
Neff DAgostino Percutaneous Access 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 (Food)·F-1954-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish and Razor Clams
Northwest Wild Products is recalling canned fish and razor clams with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Columbia River Chinook Salmon -Custom Smoked, NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1965-2016·2016-08-31
Northwest Wild Products Recalls Canned Fish and Razor Clams for Botulism Risk
Northwest Wild Products is recalling canned fish and razor clams with codes starting with OC due to potential Clostridium botulinum contamination.
Product
Oregon Sardines - Custom Smoked-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-1467-2016·2016-08-31
Mylan Amlodipine Besylate Tablets Recalled for CGMP Deviations
Mylan Institutional, Inc. is recalling Amlodipine Besylate Tablets, 5 mg, because they were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Product
Amlodipine Besylate Tablets, USP, 5 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-451-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-451-56, c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-451-19; and d)…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1959-2016·2016-08-31
Northwest Wild Products Recalls Canned Seafood Due to Botulism Risk
Northwest Wild Products is recalling various canned seafood products due to potential Clostridium botulinum contamination.
Product
Oregon Sardines - Spicy Tomato-NW Wild Products, 6.5 oz. metal cans. No UPC
Category
Food
Distribution
1 state
SevereNHTSA·16E069000·2016-08-29
Idle Free Systems Recalls Auxiliary Power Units Due to Fire Risk
Idle Free Systems is recalling 507 Auxiliary Power Units with Reefer-type trailer Link Kits manufactured between 2010 and 2016. The battery positive cable may short to ground, increasing the risk of a fire.
Product
ELECTRICAL SYSTEM:WIRING recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V626000·2016-08-29
KME Fire Trucks Recalled for Potential Driveshaft Failure
Kovatch Mobile Equipment is recalling 56 KME fire trucks because replacement driveshafts may twist and fail, potentially immobilizing the vehicle.
Product
KME — KME PREDATOR SS PUMPER, FDNY PUMPER
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·075-2016·2016-08-26
WFSP Foods Recalls Pork and Chicken Sausage Due to Undeclared Milk Allergen
WFSP Foods LLC is recalling approximately 18,672 pounds of Land O Frost sausage products because the packaging fails to declare milk, a known allergen.
Product
WFSP Foods LLC — WFSP Foods, LLC Recalls Pork and Chicken Sausage Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·16V625000·2016-08-26
Horton Ambulances Recalled for Air Conditioner Wiring Fire Risk
Halcore Group is recalling 2013-2016 Horton ambulances because a poorly sealed air conditioner wire harness allows water entry, creating a risk of electrical fire.
Product
HORTON AMBULANCE — HORTON AMBULANCE 453, 457, CHANGE OVER, 623
Category
Vehicle
Distribution
Distributed nationwide

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23376–23400 of 39702