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
E3 Artisan is recalling Meltaway bar-black cherry lemonade dark chocolate bars because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaways dark chocolate bars because FDA testing found undeclared milk. Consumers with allergies should not consume the product.
E3 Artisan is recalling dark chocolate bars with strawberries, rose petals, and pink peppercorns because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaway bars because FDA samples tested positive for undeclared milk, posing a risk to consumers with milk allergies.
E3 Artisan is recalling dark chocolate bars containing strawberries, mangoes, and chiles because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, posing a risk to consumers with milk allergies.
E3 Artisan is recalling 40 bars of 3-piece Blood Orange Meltaways because FDA samples tested positive for undeclared milk.
Volvo is recalling 2016-2017 VNL, VNX, and VNM trucks because a missing roll pin or loose bolt may cause the steering shaft to separate, resulting in a loss of steering.
E3 Artisan is recalling Meltaway bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling specific dark chocolate bars because FDA samples tested positive for undeclared milk, a major allergen.
Goodman Company is expanding a recall for specific air conditioning and heating units because their power cords can overheat, posing fire and burn risks.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
E3 Artisan is recalling Mendiant dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling specific dark chocolate bars because FDA testing found undeclared milk, a major food allergen.
Mevion Medical Systems is recalling four MEVION S250 Radiation Therapy Systems because the treatment table positioning belt can slip, causing patient setup deviations.
E3 Artisan is recalling dark chocolate bars because FDA testing found undeclared milk, a major allergen, in the product.
E3 Artisan is recalling 30-bar packages of Tahitian Vanilla Lemon Meltaways because FDA testing found undeclared milk on the labels.
E3 Artisan is recalling dark chocolate bars containing candied ginger, orange peel, and coriander because FDA samples tested positive for undeclared milk.
E3 Artisan is recalling Meltaway bars because FDA samples tested positive for undeclared milk, a major food allergen.
Philips is recalling two Allura Xper FD OR Tables because the C-arc may continue moving after stopping due to improper adjustment.
Pharmedium Services, LLC is recalling 19 syringes of Morphine Sulfate in Wisconsin because the drug was found to be subpotent.
C.R. Bard is recalling Arctic Sun 5000 and 2000 devices because a simulator key could be connected to the patient cable, resulting in improper temperature therapy.
E3 Artisan is recalling 3-piece peppermint meltaways because FDA samples tested positive for undeclared milk.
Smith & Nephew is recalling BEAVER Blade 4.0mm orthopedic instruments because they may fracture during hip arthroscopy procedures.
FreshPoint Corporate is recalling sliced cucumbers in Florida and Georgia due to possible Salmonella contamination.