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
Medline is recalling specific lots of Cataract Preop Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could allow contamination.
Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alerts, which may delay clinical evaluation.
AVID Medical, Inc. is recalling 11,763 Halyard medical convenience kits due to potential unexpected variability in endotoxin levels.
Medline is recalling 434,595 convenience kits nationwide due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Medline Industries is recalling 58,037 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that may allow contamination.
Medline is recalling convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.
Baxter Healthcare is voluntarily recalling MYXREDLIN insulin due to CGMP deviations. The recall covers specific lots distributed in the US, Puerto Rico, and Chile.
Medline is recalling 22,736 IV start kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Ford is recalling 2026-2027 Transit vehicles because the rear seat belt reminder system may malfunction, failing to alert occupants if a seat belt is unfastened.
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alerts, which may delay clinical evaluation.
Medos International Sarl is recalling 29 Velys Robotic-Assist Stations due to a software issue that may cause unintended robotic arm movement during surgery.
Medline is recalling 13,032 pre-operative kits nationwide due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Medline is recalling IV start kits containing BD ChloraPrep applicators with potentially open or incomplete seals, which may lead to infection.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Medline is recalling 4,636 convenience kits nationwide due to packaging wrinkles that may compromise sterility, posing a risk of microbial contamination.
Prince Bakery Inc is recalling 150 units of Italian and French bread in New York because sesame is not declared in the ingredient statement.
Allies Group Inc. is recalling 29,014 tubes of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Wonton Specialist is recalling 16 oz Lo Mein Noodles sold in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Wonton Specialists is recalling 16 oz wonton skins sold in NY, NJ, and PA due to undeclared FD&C Red No. 40.
Allies Group Inc. is recalling 27,492 sachets of THE ONE SPF 50 Invisible Sunscreen Gel because firm testing indicated the product may not reliably provide the stated SPF 50 protection.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate for Bicarbonate Hemodialysis due to reports of blue-green discoloration in the product.
Lexia LLC is recalling Broadway Joe's Pain Cream in Colorado due to potential raw material contamination.