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
Redline Pharmacy Solutions is recalling Morphine Sulfate (MITIGO) 5 mg/mL intrathecal syringes due to a lack of processing controls.
Redline Pharmacy Solutions is recalling 8 doses of Ertapenem Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.
Domino Foods Inc. is recalling Great Value Pure Granulated Sugar because it may contain metal pieces. The product was shipped to one consignee in Pennsylvania.
Maryland Packaging, LTD. is recalling 4,056 bags of Pure Cane Granulated Sugar in Pennsylvania and Maryland because the product may contain a metal wire.
Tova Industries is recalling Shaver Foods brand Gravy Beef because of possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.
Heartware, Inc. is recalling 5,489 HeartWare HVAD System Battery Chargers because users may mistakenly insert the AC adapter into the HVAD Controller power port.
American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.
Yokohama is recalling specific commercial tires where the tread or bead may detach, potentially causing loss of vehicle control.
Volkswagen Group of America is recalling 2017-2019 Audi Q7 and 2019 Q8 vehicles because a steering shaft bolt may loosen, potentially causing a loss of steering control.
Tornel is recalling specific Deportiva tires where adhesive failure may cause tread separation, increasing the risk of vehicle control loss and crashes.
General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch wires may fracture, allowing the hood to open while driving.
Blendtopia is recalling Superfood Smoothie Kit Glow flavor pouches due to potential Listeria monocytogenes contamination. Consumers should stop using the product.
Blendtopia Products, LLC is recalling Superfood Smoothie Kit Energy flavor pouches due to potential Listeria monocytogenes contamination.
Blendtopia Products, LLC is recalling Superfood Smoothie Kit Strength flavor pouches due to potential Listeria monocytogenes contamination.
Blendtopia is recalling Superfood Smoothie Kit Detox flavor pouches due to potential Listeria monocytogenes contamination. Consumers should stop using the product.
Axia Pharmaceutical is recalling Methylprednisolone Acetate/Bupivacaine Injectable Suspension due to a lack of assurance of sterility.
Axia Pharmaceutical is recalling specific lots of Triamcinolone Diacetate Injectable Suspension because the product lacks assurance of sterility.
Axia Pharmaceutical is recalling specific lots of Mitomycin-C Irrigation Solution because the FDA cannot assure the sterility of the product.
Axia Pharmaceutical is recalling B-Complex 110 Injectable vials due to a lack of assurance of sterility. The affected lots were distributed nationwide and in several international locations.
Axia Pharmaceutical is recalling Dexamethasone (LA) Injectable Suspension because the product lacks assurance of sterility. The recall covers specific lots distributed in the U.S., Puerto Rico, Barbados, and the Dominican Republic.
Fusion IV Pharmaceuticals is recalling specific lots of Pyridoxine Hydrochloride Injection due to a lack of assurance of sterility. The product was distributed nationwide and in several Caribbean territories.
Axia Pharmaceutical is recalling specific lots of Human Chorionic Gonadotropin (hCG) Injection due to a lack of assurance of sterility.
Axia Pharmaceutical is recalling Alprostadil/Papaverine/Phentolamine Injection due to a lack of assurance of sterility. The product was distributed nationwide and in Puerto Rico, Barbados, and the Dominican Republic.
Pfizer is recalling 24,714 vials of Elelyso (taliglucerase alfa) for injection due to reports of loose metal ferrule crimps that compromise sterility.
Axia Pharmaceutical is recalling Lidocaine HCL Injection due to a lack of assurance of sterility. The product is distributed in the U.S., Puerto Rico, Barbados, and the Dominican Republic.