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.
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.
Minimum severity
Jac Vandenberg Inc. is recalling Rio Duero plums sold at ALDI due to potential Listeria monocytogenes contamination.
Edwards Lifesciences is recalling 459 Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings, potentially leading to misdiagnosis.
Edwards Lifesciences is recalling 9 units of Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings.
Jac Vandenberg Inc. is recalling bulk peaches from Chile and Rio Duero brand peaches sold at Aldi due to potential Listeria monocytogenes contamination.
Dakota Specialty Milling is recalling Enhanced Flax Flour Blend because an ingredient may be contaminated with Salmonella. The product was distributed in California, Ohio, and Texas.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable limits.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA) above acceptable levels.
Prinston Pharmaceutical Inc is recalling Irbesartan and Hydrochlorothiazide tablets because FDA labs found the impurity NDEA above acceptable levels.
Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found N-nitrosodimethylamine (NDEA) above the acceptable daily intake level.
Aisin World Corp. of America is recalling Transmission Control Modules for 2016-2019 Mazda Miata MX-5 and 2017-2019 Fiat 124 vehicles. Incorrect programming may cause unexpected downshifting and abrupt deceleration.
West Pharma Services IL, Ltd. is recalling Vial2BAG DC 13mm devices due to reported adverse events and potential inadequate drug admixing.
Prinston Pharmaceutical Inc. is recalling Irbesartan 300 mg tablets because FDA testing found N-nitrosodimethylamine (NDEA) levels above the interim acceptable daily intake.
Subaru is recalling 2019 Forester and Crosstrek vehicles because a steering connector may short circuit, causing a loss of power steering assistance.
Edwards Lifesciences is recalling 875 units of Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings.
Lupin Pharmaceuticals is recalling 14,400 bottles of Cephalexin for Oral Suspension due to CGMP deviations and the presence of extraneous material in sucrose excipients.
Richwell Group is recalling approximately 73,360 pounds of frozen Sheat fish products that were imported from Vietnam without the required benefit of import inspection.
Hyundai is recalling 2011-2013 Tucson vehicles because the engine oil pan may leak, potentially causing engine damage, fire, or stalling.
Chrysler is recalling 2019 Ram 1500 trucks with adjustable pedals because the brake pedal may separate from the assembly, increasing crash risk.
Chrysler is recalling 2017-2019 Fiat 124 Spider vehicles with automatic transmissions due to a software defect that may cause unexpected downshifting and sudden deceleration.
Q's American Best Trading Inc. is recalling approximately 1,008 pounds of imported frozen Sheat fish products that were not presented for import re-inspection.
Pilgrim's Pride is recalling approximately 58,020 pounds of frozen, uncooked breaded popcorn chicken products due to possible contamination with rubber.
Mazda is recalling 2016-2019 MX-5 vehicles with automatic transmissions because incorrect software may cause unexpected downshifting and abrupt deceleration.
Forest River is recalling 2019 Rockwood and Flagstaff trailers because improper wiring may prevent brakes from engaging if the trailer disconnects from the tow vehicle.
Daimler Vans is recalling 2019 Mercedes-Benz Sprinter VS30 vehicles because the steering shaft may disconnect, causing a sudden loss of steering control.
Happy Together, Inc. is recalling 5K Premium Enhancement capsules because FDA analysis found undeclared sildenafil and tadalafil.