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
AstraZeneca is recalling 40,368 bottles of BRILINTA 90 mg tablets because some bottles contained foreign Zurampic tablets.
SCA Pharmaceuticals is recalling 660 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Oscor, Inc. is recalling ATAR Reusable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Baxter Healthcare is recalling 0.9% Sodium Chloride Injection bags due to customer complaints about leaking bags, which raises concerns about the product's sterility.
Sigan Industries is recalling CVS Health Baby Eczema Moisturizing Cream due to microbial contamination. The product failed to meet total plate count specifications.
Samiira's Homemade Muhammara Roasted Red Pepper Dip is being recalled because it may contain undeclared soy. Consumers should stop using the product.
Publix is recalling Tropical Fruit Medley due to the possible presence of Listeria monocytogenes. Consumers should discard the product.
Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Oscor, Inc. is recalling ATAR Disposable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.
LJA Enterprises is recalling Sweet and Spicy Mix bags in Ohio due to undeclared milk, soy, and wheat allergens.
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.
SCA Pharmaceuticals is recalling 221 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.
Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.
LJA Enterprises is recalling 15 bags of Nutman Hunter Trail Mix because the product failed to declare milk as an ingredient.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
Mazda is recalling specific 2007-2012 CX-7, CX-9, and Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.
Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 transit buses because the wheelchair pocket track anchorage may not secure a wheelchair in a crash.
Daimler Trucks North America is recalling 2014-2017 Freightliner Custom Chassis XCR vehicles because an improperly installed battery cable bracket may cause a short circuit and fire.
Nissan is recalling 2007-2012 Versa vehicles because the driver's air bag inflator may rupture, potentially causing serious injury or death.