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 deaths or serious injuries are reported, 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
Jayco is recalling 2025 Entegra Launch and Terrain motorhomes because a standard outlet was installed in the kitchen instead of a GFCI protected outlet, increasing the risk of electric shock.
USDA FSIS issued a public health alert for raw ground beef sold by Bismillah Halal Meats in Georgia due to possible E. coli O103 contamination.
USDA FSIS issued a public health alert for mixed potato chip products containing pork cracklings imported from Colombia, a country ineligible to export meat to the U.S.
Abbott is recalling the Amplatzer TorqVue LP Catheter (Model 9-TVLPC4F90/080) due to a potential small breach in the proximal shaft that may not be visible and could lead to prolonged procedures, blood loss, or air embolism.
Leiters Health is recalling dexmedetomidine HCl PF syringes nationwide due to leaking or damaged syringes that may not maintain sterility. Affected lot 2431276A has an expiration date of 4/20/2025.
Denver Solutions, LLC is recalling Ketamine HCl 50mg per 5mL single-dose syringes nationwide due to leaking or damaged syringes that may lack sterility assurance. Two affected lots are identified with expiration dates in July 2025.
Denver Solutions, LLC DBA Leiters Health is recalling Rocuronium Bromide 50 mg per 5mL syringes due to potential leaking or damage that may compromise sterility assurance.
Zaarah Herbals brand Gurmar Powder is being recalled due to elevated lead levels. The product was distributed in New York, Connecticut, New Jersey, and California.
Denver Solutions, LLC DBA Leiters Health is recalling PHENYLephrine HCl 0.5 mg per 5mL single-dose syringes because some syringes may be leaking or damaged, which could compromise sterility assurance.
Conavi Medical Inc. is recalling the Novasight Hybrid Catheter (Model TA-06-0001) due to manufacturing issues that could cause the catheter sheath to detach. The device is used for diagnostic intravascular imaging.
Abbott is recalling specific lots of the Amplatzer TorqVue LP Delivery System due to a possible small breach in the shaft that is not visible but could lead to prolonged procedures, blood loss, or air embolism.
Zaarah Herbals brand Bhringraj Powder contains elevated levels of lead and arsenic. Consumers should not use the product and should contact the recalling firm for instructions.
Walker's Wine Juice Pumpkin Juice in 2.5, 5, 30, 60, and 275 gallon bulk containers is being recalled due to potential contamination with Clostridium botulinum. The product was distributed across multiple states.
Zaarah Herbals brand Vasaka Powder is recalled due to elevated lead levels of 6.504 ppm. The product was distributed in New York, Connecticut, New Jersey, and California.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The drug is used for intramuscular injection to treat psychiatric conditions.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection vials nationwide because some media fill units showed bacterial contamination, indicating a lack of sterility assurance. The affected product is a 100mg/mL injectable antipsychotic medication.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The affected product was distributed nationwide.
Zaarah Herbals brand Rasayan Churan (100g jars) is recalled due to elevated lead levels of 88.038 ppm. The product was distributed in New York, Connecticut, New Jersey, and California.
Cromer Food Services is recalling chicken salad sandwiches because milk was not declared on the label. Consumers with milk allergies are at risk.
Request Foods Incorporated is recalling Cuban-Style Black Bean Soup due to potential contamination with wood. The product was distributed in Illinois and Michigan.
Philips is recalling Zenition 70 radiological systems with wireless foot switches that may stick in the active position when released, potentially causing unintended radiation emission during medical procedures.
Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.
S Martinelli & Company is recalling approximately 7,234 cases of apple juice in 10 oz bottles due to potential contamination with patulin. Consumers who have purchased affected product should not consume it.
Supplement Manufacturing Partner Inc. is recalling Spermidine Maximum Strength 10 mg dietary supplement (Lot 12792402-44) because it contains undeclared wheat, a major allergen not listed on the label.
Philips is recalling Zenition 70 systems with Vascular Extension option and Wireless Foot Switch due to potential for unintended radiation exposure in healthcare facilities.