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
Ford is recalling specific 2014 Focus, 2014 Escape, and 2015 Lincoln MKC vehicles because a fuel delivery module may crack, causing low fuel pressure and potential vehicle stalls.
Ford is recalling 2015 F-650 and F-750 SD trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Mitsubishi is recalling 2010-2014 i-MiEV electric vehicles because the brake vacuum pump may stop functioning, potentially increasing stopping distance and crash risk.
Genera is recalling specific aftermarket headlamp assemblies for 2013-2014 Acura ILX vehicles due to overheating risks that could cause smoke, melting, or fire.
Gillig is recalling 231 model year 2014 Low Floor transit buses because a fuel filter defect may cause the engine to stall unexpectedly, increasing the risk of a crash.
New Flyer is recalling 2014 transit buses because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.
General Motors is recalling specific 2013-2014 Cadillac XTS and Chevrolet Impala vehicles because the air bag control module may be in manufacturing mode, preventing deployment in a crash.
Baxter Healthcare is recalling 4,200 containers of 0.9% Sodium Chloride Injection because blue polyisoprene shavings were found inside the bag port tubes.
The TJX Companies is recalling approximately 150 units of ecoato Sweet Paprika Powder because of a potential Salmonella contamination risk.
Natural Grocers by Vitamin Cottage is recalling Chunks of Energy products due to the potential presence of Salmonella.
Pharmacy Creations is recalling 70 vials of Ascorbic Acid 500 mg/mL sterile injection due to mold contamination. The affected product was distributed in New York, New Jersey, and Puerto Rico.
Ciranda, Inc. is recalling one lot of Organic Carob Powder Light after a customer reported a positive Salmonella test.
Ben Venue Laboratories is recalling 7,172 vials of Cytarabine for Injection due to potential crimp defects that may affect sterility.
AngioDynamics is recalling Uni*Fuse Infusion Systems with Cooper Wire because they may contain a guidewire that is too long.
Healix Infusion Therapy is recalling 50 fentanyl syringes because the supplier recalled the drug due to loose or missing vial crimps, raising sterility concerns.
Tnuva USA is recalling approximately 8,316 pounds of Mom's Chicken Extra Thin Cutlets due to possible Listeria monocytogenes contamination. No illnesses have been reported.
CaCoCo, Inc. is recalling specific lots of Superfood Drinking Chocolate because an organic ingredient used in the product is under recall for potential Salmonella contamination.
Ortho Development is recalling specific knee implant components because defective foil pouches allowed air to enter, potentially degrading the material properties of the implants.
Childrens Medical Ventures is recalling Gel-E Donut and Squishon 2 gel pillows because of visible mold. The mold was identified as Cladosporium and Penicillium fungi.
Healix Infusion Therapy is recalling 220 fentanyl prefilled syringes because the supplier recalled the drug due to loose or missing vial crimps, raising sterility concerns.
Goodman Company is recalling approximately 233,500 packaged terminal air conditioners and heat pumps because power cords can overheat, posing fire and burn risks.
Synthes, Inc. is recalling specific lots of the DePuy Synthes Craniomaxillofacial Distraction System because the devices may reverse after surgery.
Hospira Inc. is recalling 123,900 vials of Dobutamine Injection due to the presence of glass particulate matter and a discolored solution.
Healix Infusion Therapy is recalling 48 bags of compounded fentanyl in Texas and Georgia because the supplier recalled the source drug due to loose or missing vial crimps.
Healix Infusion Therapy is recalling 12 bags of compounded fentanyl and ropivacaine due to a lack of assurance of sterility from a supplier recall.