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
eBars is recalling 48,969 units of MAN Organic Chocolate Almond bars because they tested positive for peanut, an undeclared allergen.
Apotex Inc. is recalling specific lots of Piperacillin and Tazobactam for Injection due to high impurity levels that decreased the drug's potency.
Medtronic is recalling 171,271 Endo GIA Bypass Kits because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Medtronic is recalling Endo GIA universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
eBars is recalling FOCUS Organic Chocolate Peanut bars because they contain undeclared almonds. The recall affects 33,115 units shipped to multiple states.
Medtronic is recalling Endo GIA Universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Columbia Northwest is recalling 2016-2017 Somerset Newport and Chesapeake trailers because a front weld may fail, causing the trailer to drop and increasing crash risk.
Hempler Foods Group is recalling ready-to-eat pepperoni sticks because they contain milk, a known allergen, that is not declared on the label.
Van-Con is recalling one 2016 33803 Dual Rear Wheel school bus because roof panel seams were not correctly bonded, posing an increased injury risk in a crash.
Chrysler is recalling over 4.8 million vehicles because a wiring short may prevent the cruise control system from disengaging, increasing crash risk.
Tiffin is recalling 2013-2018 Allegro Open Road motorhomes because weak frame rails may allow the tow hitch to detach, increasing crash risk.
Setra is recalling 2017-2018 S417 TC and S407 CC motorcoaches because a steering drop arm nut may loosen, potentially causing a loss of steering control.
LuK is recalling hybrid propulsion systems where oil accumulation may cause an electrical short and increase fire risk. Dealers will inspect and replace components free of charge.
Triangle Pharmanaturals LLC is recalling Molecule Kratom Red Malay products due to potential Salmonella contamination. The products were distributed in 24 states.
Eden's Ethnos LLC is recalling 2,775 kilograms of bulk Kratom powder because FDA and state samples found Salmonella. The product was distributed in five states.
Triangle Pharmanaturals LLC is recalling Molecule Kratom Red Maeng Da products due to potential Salmonella contamination.
Triangle Pharmanaturals LLC is recalling Naturally Kratom Red Malay capsules because all Kratom products from the firm may be contaminated with Salmonella.
Badger Botanicals LLC is recalling specific Kratom products due to potential Salmonella contamination. Consumers should stop using these items.
Triangle Pharmanaturals LLC is recalling Third Eye Kratom Red capsules because all Kratom products from the company may be contaminated with Salmonella.
Triangle Pharmanaturals LLC is recalling Molecule Kratom Green Maeng Da products due to potential Salmonella contamination. The recall covers multiple package sizes distributed across 24 states.
Badger Botanicals LLC is recalling specific Kratom products due to potential Salmonella contamination.
Labrada Nutrition is recalling 132 units of Lean Pro 8 Cookies & Cream protein powder due to undeclared egg. The product was distributed in the US and internationally.
Maya Distribution, LLC is recalling Dragon Maeng Da Kratom Powder and capsules because samples tested positive for Salmonella. The product was sold in eight states.
Triangle Pharmanaturals LLC is recalling Chameleon Kratom Formula 51 capsules because all Kratom products from the firm may be contaminated with Salmonella.
Triangle Pharmanaturals LLC is recalling Molecule Kratom White Maeng Da products in various formats due to potential Salmonella contamination.