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
Pfizer is recalling 53,600 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass vials.
Blue Moose of Boulder, LLC is recalling 504 units of All-Natural Ciolo Nut-Free Basil Pesto because the product contains undeclared tree nuts.
Alden Optical is recalling 23 units of HP49 Sphere Daily Wear Soft contact lenses because they lack sterility assurance.
Maxey Trailers is recalling 2017-2018 A3X, A5X, and A6X trailers because suspension arms may crack, potentially causing the axle to come loose and increasing crash risk.
Plant Devas Inc. is recalling Blemish Face Care Kits because FDA sampling found excessive and virulent microorganisms.
Plant Devas Inc. is recalling 144 units of Ayurvedic Face Care Kits because FDA testing found excessive numbers of microorganisms.
Alden Optical is recalling specific daily wear soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.
Sagent Pharmaceuticals is recalling 176,410 vials of methylprednisolone sodium succinate injection due to high impurity levels.
Pfizer is recalling 29,680 vials of Hydromorphone Hydrochloride Injection due to confirmed customer complaints of empty or cracked glass containers.
Alden Optical is recalling NovaKone Daily Wear Soft contact lenses because they lack sterility assurance. The recall covers units distributed in the US and Canada.
Smiths Medical ASD Inc. is recalling certain Port-A-Cath II kits that may contain incorrect introducer sizes or locking collars due to misassembly.
Progressive Laboratories is recalling Xenesta Nuvive Women's 90-count bottles due to potential undeclared milk content.
Sunneen Health Foods is recalling 60 units of Vegan Buffalo Chicken Bites because the label fails to declare pecans.
Forest River is recalling 2018 Surveyor trailers because a missing fan in the refrigerator may cause overheating and fire.
Sagent Pharmaceuticals is recalling methylprednisolone sodium succinate for injection vials due to high impurity levels. The affected lots were distributed nationwide.
Progressive Laboratories is recalling Testosterzone dietary supplements because they may contain undeclared milk, a major food allergen.
Plant Devas Inc. is recalling 500 kits of the evanhealy Clay Mask Kit because FDA testing found excessive and virulent microorganisms.
Plant Divas Inc. is recalling Green Tea Clay because FDA testing found excessive and virulent microorganisms in the product.
Progressive Laboratories is recalling Xenesta Nuvive Men dietary supplements because they may contain undeclared milk.
Alden Optical is recalling ASTERA Multifocal Toric Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.
Plant Divas Inc. is recalling French Rose Clay and Moroccan Rhassoul Clay products because FDA testing found excessive numbers of microorganisms.
Argo Medical Technologies is recalling 127 ReWalk Personal 6.0 exoskeletons after receiving complaints of tibia and fibula injuries.
Alden Optical is recalling HP59 Toric Daily Wear Soft contact lenses because they lack sterility assurance. Consumers should stop using the affected lenses.
Sagent Pharmaceuticals is recalling 205,370 vials of methylprednisolone sodium succinate for injection due to high impurity levels.
Progressive Laboratories is recalling Thyroid Resilience dietary supplements because they may contain undeclared milk. Consumers should stop using the product and return it to the place of purchase.