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 deaths or serious injuries are reported, 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
Biomet, Inc. is recalling various sizes of Intramedullary Bone Saw Blade Assemblies because an exposed saw blade may have damaged the sterile barrier packaging.
United Orthopedic Corp. is recalling specific femoral valgus offset adaptors used in the U2 Total Knee System due to a manufacturing defect in a component screw.
Beckman Coulter Biomedical GmbH is recalling REMISOL Advance Software Version 2.5 because it may incorrectly report combo assay test outcomes.
Stryker is recalling 11,857 Single Spike Tube Sets due to reports of leaking from the handpiece during use.
La Colonia Foods LLC is recalling 19 units of Requeson cheese packed in 18-lb buckets due to possible contamination with Listeria monocytogenes. The product was distributed to MD and VA.
Tissium SA is relabeling Coaptium Connect nerve repair devices because the current 36-month shelf life is not supported by real-time data. The shelf life is being reduced to 26 months.
A recall has been issued for the Quantum 4Front 2HD powered wheelchair because its controller software may cause unexpected braking or system failure that could lead to falls or injury.
Eunha Fisheries Co., LTD is recalling Sliced Korean Halibut due to undeclared allergens including wheat, soy, and sesame.
Volvo Trucks is recalling certain Grote replacement marker lights that may fail to illuminate, reducing vehicle visibility and increasing crash risk.
Pride Mobility Products Corp. is recalling 1,102 Quantum 4Front 2 wheelchair controllers because reminder pop-ups can trigger unexpected park brake stops while driving, causing falls or injuries.
Tissium SA is relabeling COAPTIUM Connect nerve repair devices to reduce the shelf life from 36 to 26 months because the original duration was not supported by real-time data.
Mack Trucks is recalling certain Grote replacement marker lights that may fail to illuminate, reducing vehicle visibility and increasing crash risk.
Zimmer Biomet recalls Intramedullary Bone Saw Blade Assemblies due to potential sterile barrier packaging damage from exposed saw blades. FDA Class II medical device recall.
Tissium SA is relabeling COAPTIUM CONNECT nerve repair devices because the 36-month shelf life is not supported by real-time data. The revised shelf life is 26 months.
Pride Mobility is recalling 1,102 Q6 Edge 2.0 power wheelchairs due to a software issue that may cause unexpected braking or control system crashes during use.
Integrated Medcraft is recalling specific Kingfisher Compact Individual First Aid Kits because the included Guedel airway components may have occluded tips.
Clover Hill Dairy, LLC is recalling its sharp cheese varieties due to potential contamination with Listeria monocytogenes. The recall affects products distributed in MD, VA, and NY.
M.G. Foods, Inc. is recalling Spicy Breakfast Burritos because they contain undeclared soy in the sausage component.
Pack'n Fresh LLC is recalling various lots of Hondashi 0.25oz seasoning because the product contains fish that is not listed in the ingredients statement.
La Colonia Foods LLC is recalling 169 units of Selectos Latinos Requeson Mexicano Mexican Cottage Cheese (16 oz) due to potential contamination with Listeria monocytogenes. The product was distributed in MD and VA.
Siemens Healthcare Diagnostics is recalling Atellica CH Urine Albumin assays due to potential false results and QC failures when processed on CI analyzers.
Aniara Diagnostica LLC is recalling 5-PLASMA Bivalirudin Control (Model 5D-44905) due to stability issues that may cause degradation of measurable bivalirudin.
PT Organics Limited is recalling certain Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree pouches due to the potential presence of thin, soft plastic strands.
Central Admixture Pharmacy Services is recalling two patient-specific pediatric TPN bags due to incorrect product formulation. The recall affects lots 20-1535990-0-1 and 20-1535892-0-1 with an expiration date of July 16, 2026, distributed in Georgia only.
Happiest Baby, Inc is recalling 4 refurbished SNOO Smart Sleeper bassinets (Model S1000) that failed to meet quality standards before distribution. The recall is being reported retroactively.