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
Abiomed is recalling the Impella RP Flex cardiac assist device because its differential pressure sensor may malfunction and drift, potentially affecting device function. The FDA classified this as a Class I recall.
SILINTAN 25 pills, sold nationwide, contain meloxicam but lack FDA approval. The manufacturer sold the product without the required drug application.
Abiomed is recalling 179 Impella RP devices worldwide due to a differential pressure sensor that may malfunction and cause sensor values to drift. The FDA has classified this as a Class I recall.
Mylan Pharmaceuticals is recalling Amnesteem (isotretinoin) 40 mg capsules due to failed dissolution specifications, which may affect medication effectiveness. The recall affects 34,850 blister packs distributed nationwide.
Teva Pharmaceuticals is recalling 7,448 bottles of Metoprolol Succinate Extended-Release 100 mg tablets nationwide due to failed dissolution specifications. The defect could result in inadequate drug absorption. Contact your pharmacist if you have affected lots.
Siemens is recalling Atellica CH Urine Albumin test kits due to measurement error producing falsely low results. Samples with urine albumin above 40.0 mg/dL may report 6.2-40.0 mg/dL, affecting 4,885 units worldwide.
B. Braun has recalled 51,300 units of its 21GA Winged Infusion Set due to potential needle defects. The needle tips may be dull, blunt, difficult to advance, or prone to breaking during use.
A software defect in Roche's cobas pro automated diagnostic analyzer allows erroneous calibrations, causing the system to repeat previous results instead of calculating new values, potentially leading to incorrect patient lab results.
B. Braun is recalling approximately 105,550 BBraun Medical 21G X4.4CM Winged Infusion Needles due to potential for needle tips to be dull, blunt, or prone to breaking.
Volkswagen is recalling certain 2022 Audi A7 PHEV vehicles because the high-voltage battery may overheat, increasing the risk of fire. Owners should not charge their vehicles until the final remedy is available.
Olympus recalled ShockPulse-SE Lithotripsy Systems where the generator fails to recognize the transducer probe. The issue affects 1,082 units distributed worldwide.
The FDA is recalling Midodrine Hydrochloride 5mg tablets due to defective, inadequately sealed blister packaging. The recall affects 8,892 cartons distributed nationwide.
Vascutek vascular prostheses (Gelsoft Plus and Gelweave) were mislabeled with incorrect expiration dates, with devices marked to expire one month later than they actually will. The labeling used packaging date instead of gel impregnation date for shelf-life calculation.
Harbin Jixianglong Biotech is recalling semaglutide raw ingredient used for pharmacy compounding due to incomplete process and endotoxin testing validation before distribution.
New Life Pharma LLC recalled 45 vials of Tirzepatide 15mg injectable due to lack of assurance of sterility. The affected lot was distributed in Ohio.
Acme United Corporation is voluntarily recalling First Aid Only Hand Sanitizing Wipes nationwide due to manufacturing process deviations. No injuries or illnesses have been reported.
Lidocaine cream lacking stability data to support its expiry date is being recalled nationwide. Consumers should stop using affected bottles and consult their pharmacist.
ACME UNITED CORPORATION has voluntarily recalled Wipes Plus hand sanitizing wipes due to CGMP deviations. No illnesses have been reported.
New Life Pharma LLC is recalling Semaglutide 2mg sterile injectable vials due to lack of assurance of sterility. Two lots distributed in Ohio are affected.
Radnostix recalls Sodium Iodide I-131 oral solution (FDA Class II) due to particulate matter contamination from production issues. Affected product was distributed nationwide in the USA and Puerto Rico.
Teva Pharmaceuticals is recalling 67,043 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg nationwide due to failed dissolution specifications. Affected tablets may not release medication properly in the body.
Teva Pharmaceuticals recalls Metoprolol Succinate Extended-Release Tablets (200 mg) due to failed dissolution specifications. The recall affects 19,056 bottles distributed nationwide.
Olympus is recalling its Single Use Biopsy Valve (Model MAJ-1218) due to potential rubber fragments detaching during use. The product has been distributed nationwide.
Teva Pharmaceuticals is recalling 18,780 bottles of metoprolol succinate extended-release tablets nationwide due to failed dissolution specifications that may reduce medication effectiveness.
ACME UNITED CORPORATION is recalling WP WipesPlus Hand Sanitizing Wipes nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The company voluntarily initiated the recall following FDA notification.