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
Global Marketing Enterprises is recalling 52.5 kg of unapproved caffeine powder marketed with stimulant claims and lacking adequate directions for use.
Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.
ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.
Boston Scientific is recalling approximately 12,450 SQ-RX 1010 Pulse Generators because memory corruption may cause the device to deliver an atypical amount of energy.
Boston Scientific is recalling approximately 16,750 Emblem S-ICD devices because they may deliver atypical energy levels due to internal memory corruption.
Laura's Boston Brownies is recalling specific lots of Bhufit Bar Superfood Chocolate Chip Brownie Batter due to potential Listeria monocytogenes contamination.
Toyota is recalling 2017 Highlander and Highlander Hybrid vehicles because roof rail fasteners may not be torqued properly, posing a road hazard risk.
Forest River is recalling 2018 Rockwood and Flagstaff trailers because improperly torqued spindle nuts may cause hub bearing failure and loss of vehicle control.
Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.
Nutrilife is recalling 29% hydrogen peroxide bottles because caps may not vent properly, allowing pressure to build and cause rupture, posing fire and burn risks.
NatureAll-STF Holding, LLC is recalling 254 bottles of Metabo-Plus dietary supplement because it contains undeclared milk (whey), a major allergen.
Silver Hills Bakery is recalling Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns due to undeclared eggs. The recall affects 9,639 retail units sold nationwide.
NatureAll is recalling Thymus Plus dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.
Laura's Boston Brownies is recalling Bhufit Bar Salted Caramel Pecan products due to potential Listeria monocytogenes contamination.
Sharper Image is recalling specific Emergency Car Jump Starters that may catch fire when plugged in, increasing the risk of injury.
Fair Oaks Farms is recalling fully cooked pork sausage patties due to possible Listeria monocytogenes contamination. No illnesses have been reported.
General Motors is recalling 2017-2018 GMC Acadia, 2018 Chevrolet Equinox, and 2018 GMC Terrain vehicles because the right front intermediate driveshaft may fracture and separate while driving.
Iowa Mold Tooling is recalling 2016-2017 Dominator Contractor trucks because a fuse block may contact the hood, creating an electrical short that increases fire risk.
Command Electronics is recalling specific LED ceiling lights installed in Jayco and Highland Ridge recreational vehicles because they may produce excessive heat, increasing the risk of a fire.
Blue Bird is recalling 2015-2019 Vision and 2016 All American school buses because unpadded seat studs may cause head injuries in rear crashes.
Cook Medical is recalling Zenith Alpha Thoracic Endovascular Grafts due to reports of graft thrombosis and occlusion, including one patient death.
Cantrell Drug Company is recalling 21,080 syringes of Glycopyrrolate Injection Solution due to a lack of sterility assurance.
Cantrell Drug Company is recalling Diltiazem HCl 125 mg in 5% Dextrose single-dose bags because of a lack of sterility assurance. The recall covers 2,761 bags distributed nationwide.
Cantrell Drug Company is recalling 1,718 bags of Norepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of sterility assurance.
Cantrell Drug Company is recalling 3,039 bags of Norepinephrine Bitartrate 4 mg in 0.9% Sodium Chloride due to a lack of sterility assurance.