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
New England Compounding Center is recalling Clonidine 100 mcg/mL vials nationwide due to a lack of assurance of sterility.
Forest River is recalling 2010-2012 Berkshire and Charleston diesel motorhomes because loose diode jumpers may prevent brake lights from working or cruise control from disengaging.
ARBOC is recalling 2012 Spirit of Mobility buses because passenger seat base rear bolts may be missing reinforcement plates, increasing injury risk in accidents.
Polaris is recalling 2010-2013 GEM electric vehicles because the parking brake may fail to engage, increasing the risk of the vehicle rolling away.
Praxair Inc. is recalling Vantage Grab n Go gas cylinder pressure regulators due to isolated incidents of ignition inside cylinders subjected to significant physical impact.
General Motors is recalling 54,686 model year 2013 vehicles due to a transmission defect that may allow the vehicle to roll away.
Lloyd Inc. of Iowa is recalling specific lots of Thyro-Tab 0.050 mg. tablets because they are subpotent and have a 9-month stability interval.
Zimmer, Inc. is recalling the Spine Ardis Inserter because excessive force can break the PEEK spacer, causing sharp fragments that may damage adjacent structures.
GE Healthcare is recalling T-Piece Neonatal Patient Circuit Kits because they cannot achieve maximum Peak Inspiratory Pressure during pre-use checks.
Temsa is recalling 2012-2013 TS30 motorcoaches because brake hoses may stretch and leak air when the body lift is used, reducing braking force.
Alara Pharmaceutical is recalling 7,432 bottles of Levothyroxine Sodium Tablets because the product is subpotent and has stability issues.
Brower is recalling about 2,500 Top Hatch egg incubators because the base can ignite during use, posing a fire hazard. Three fires with property damage have been reported.
Golub Corp is recalling CMC Cinnamon Coffee Cakes incorrectly labeled as Pumpkin Coffee Cake, which failed to list walnuts as an ingredient.
Spence & Co. is recalling refrigerated Nova Lox and Smoked Salmon Trimmings due to Listeria monocytogenes contamination. Consumers should discard or return these products.
F. Hoffmann-LaRoche Ltd. is recalling Cymevene 500 mg Powder for Infusion due to container closure issues that compromise sterility assurance. No product was distributed in the USA.
Taylor Farms is recalling specific bags of Hearts of Romaine Lettuce after a positive sample of Listeria Monocytogenes was found.
Lloyd Inc. of Iowa is recalling specific lots of Levothroid (levothyroxine sodium) tablets because they are subpotent and have a 9-month stability interval.
Neotek is recalling DURALAST brake rotors sold at Autozone because a narrow casting area may fracture, reducing braking performance and increasing crash risk.
Baby Matters is recalling Nap Nanny infant recliners due to design defects that pose a risk of injury and death. CPSC reports five infant deaths and numerous incidents of infants hanging or falling out.
Whole Alternatives LLC is recalling 8-ounce packages of Dried Golden Raisins due to undeclared sulphur dioxide. The product was distributed to Harris Teeter stores in nine states and D.C.
Tribe Mediterranean Foods is recalling Veggie Patch Falafel Chickpea Balls due to Listeria monocytogenes contamination. The product was distributed nationwide and in Canada.
Zimmer, Inc. is recalling 92 units of Persona Knee System Tibial Broaches and associated tools due to a risk of tibial perforation and bone fracture.
DePuy Orthopaedics is recalling Solution Calcar Stems used in hip replacements because an engineering analysis found they may impinge with certain heads, preventing them from locking as intended.
Prevost is recalling 196 model year 2011 and 2012 X3-45 coaches because a front suspension part may break, increasing crash risk.
Zimmer, Inc. is recalling Persona knee implants and associated tools to reduce the risk of tibial perforation and bone fracture.