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
Elegant Foods, LLC is voluntarily recalling 5-pound bags of Golden Raisins in Wisconsin due to undeclared sulfites.
Tiffany Food Corp is recalling Hexing Haw Balls candy because it contains the unapproved dye Ponceau 4R.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
F & A Foundation is recalling 600 units of Reign Medical Clench Staple Systems because the device's performance characteristics have not been adequately established.
Elegant Foods is recalling Carrot Cakes because the carrot decorations contain Yellow #5 and Yellow #6, which are not listed on the product label.
Taro Pharmaceuticals is recalling Lidocaine Ointment 5% due to failed content uniformity specifications during stability testing.
Wilson-Cook Medical Inc. is recalling 121,241 units of Hemospray Endoscopic Hemostat due to issues with endoscope adherence and the inability to spray powder.
Straumann USA LLC is recalling 216 GM Helix Implants because the packaging identification does not match the actual implant dimensions.
Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.
Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.
ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
Inventia Healthcare Limited is recalling 13,567 bottles of Chlorthalidone 25 mg tablets because they failed dissolution specifications. The recall is nationwide.
Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.
Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.
Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.
Ford is recalling specific 2025-2027 Expedition and F-Series Super Duty vehicles because contaminated LED chips in the headlights may cause a loss of exterior lighting, increasing crash risk.
Ford is recalling 2026 Ranger vehicles because the center screen may lose power, preventing the rearview camera image from displaying and increasing crash risk.