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
Medical Center Pharmacy is recalling Vancomycin Opthal 14 mg drops because production processes could not assure sterility. The product was distributed to patients in Tennessee.
The Medicine Shoppe Pharmacy is recalling Gentamicin 80mg/60 mL Irrigation containers due to a lack of assurance of sterility.
Medical Center Pharmacy is recalling 250 mL bags of Gentamicin/Bacitracin Bladder Irrigation due to concerns that production processes cannot assure sterility.
Medical Center Pharmacy is recalling two bottles of Mitomycin 0.04% Ophth DR eye drops because production processes could not assure sterility.
Medical Center Pharmacy is recalling specific lots of C-Albumin Eye Drop 10% S because production processes cannot assure sterility. Patients in Tennessee who received these prescriptions should contact their healthcare provider.
Tiffany Food Corp. is recalling 1,500 units of Huangfushanzhen Dried Mushroom because the product contains undeclared sulfites.
LeMaitre Vascular is recalling 5F Plus Over the Wire Embolectomy Catheters due to reports of deflation failure that may lead to tip separation.
Continuum is recalling Lenox 2.5 Quart Tea Kettles because they can expel hot water, posing a burn hazard. Consumers should stop using the kettles and contact the company for a refund.
Dr. Reddy's is recalling Phytonadione Injectable Emulsion ampules because they may break or shatter when opened.
Merits Health Products is recalling 82 E604 Pilot Navigator Stairlifts because the pinion gear may disengage from the track, allowing the lift to slip or jolt.
Stryker is recalling 1,415 Berchtold Chromophare Ceiling Mounted Surgical Light Systems because a missing snap ring or spanner nut may cause the light to fall.
Medical Center Pharmacy is recalling Morphine 2 mg/mL CADD Cassettes because production processes cannot assure sterility. Patients in Tennessee who received specific prescriptions should contact their healthcare provider.
KTM is recalling 2019-2020 790 Adventure and 790 Adventure R motorcycles because the rear brake hose may overheat, potentially causing brake failure and increasing crash risk.
Isuzu is recalling 2019 NPR and Chevrolet 4500 vehicles because incorrectly installed brake line clips may cause rear driver-side brake failure.
Isuzu is recalling 2,399 vehicles due to a wire harness routing issue that may cause stalling or ABS failure, increasing crash risk.
Southern Motion is recalling about 2,300 Wireless Power reclining furniture pieces because the lithium-ion batteries can overheat and cause fires.
Daimler Coaches is recalling 2017-2020 Setra S417TC coaches because the front entrance door support frame may be the wrong size, allowing the door to detach while moving.
Boston Scientific is recalling Imager II 5F Angiographic Catheters because the tips may detach. The recall covers 1,068,827 units distributed worldwide.
International Sprout Holding Inc. is recalling clover seed in 50 lb. bags due to possible E. Coli contamination. The product was distributed to multiple states, territories, and countries.
Thrive Pharmacy is recalling 403 buprenorphine troches in Florida because they contain less active ingredient than labeled.
International Sprout Holding Inc. is recalling 13,455 lbs of clover seed due to possible E. Coli contamination. The product was distributed to multiple US states, territories, and countries.
Medtronic MiniMed is recalling 38 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
Hong Bin Foods LLC is recalling Enoki Mushrooms after testing by the State of Michigan found Listeria monocytogenes. The product was distributed in six states.
Micro Therapeutics Inc is recalling 1,050 ev3 Pipeline Flex Embolization Devices because the delivery system may fracture during implantation, potentially leaving a part in the patient.
Thrive Pharmacy is recalling 89 Buprenorphine Black Cherry 2 mg troches in Florida because the medication was found to be subpotent.