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
Newly Weds Foods is recalling G51904 Steak and Burger Seasoning due to potential Salmonella contamination in an ingredient. Approximately 4,685 pounds were distributed to Florida, Illinois, and Texas.
Irvington Seafood is recalling Finger Crab Meat due to Listeria monocytogenes contamination identified during product testing. The recall affects 168 lbs distributed in Mississippi and Alabama.
The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.
Grande Bravo 500 Functional Whey Protein is recalled due to possible Salmonella contamination. The product was distributed across 24 US states and internationally to Canada, Ecuador, and Japan.
Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.
Kerry, Inc is recalling BrS8 RODIZIO Seas No MSG seasoning ingredient due to potential Salmonella contamination. The affected product was distributed to multiple U.S. states and Canada.
Grande Lactose (SKU 30601) is being recalled due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
GRANDE CHEESE COMPANY is recalling Grande Ultra 9100 Functional Whey Protein Isolate (SKU 32131) due to possible Salmonella contamination. The recall affects 1.7 million pounds distributed to 24 U.S. states and international markets.
Kerry Ingredients is recalling 13,341 bags of Sun Nat HV CHDR #3 SEAS food ingredient due to potential Salmonella contamination. No illnesses have been reported.
Grande Bravo 550 Functional Whey Protein is being recalled due to possible Salmonella contamination. Affected batches ANV508-1 and ANV508-3 were distributed across 24 U.S. states and internationally.
Kerry Inc. is recalling 77 bags of Cheddar & Sour Cream SEAS seasoning (lots 8092105, 8127605, 8091886) distributed across multiple U.S. states and Canada due to potential Salmonella contamination.
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.
Porsche is recalling certain 2020–2025 Taycan vehicles because the front brake hoses can develop cracks and leak brake fluid, reducing braking performance. Dealers will replace the hoses for free.
Covidien is recalling EsoFLIP 30mm balloon dilation catheters due to saline conductivity issues that may cause inaccurate esophageal measurements, potentially leading to patient harm.
Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.
Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.
B Braun Medical Inc is recalling over 1.1 million Stimuplex A nerve block needles labeled as DEHP-free, but the adhesive contains traces of DEHP. The mislabeling poses a risk to users who selected the product specifically to avoid DEHP exposure.
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.
Integra LifeSciences recalls CODMAN EVD BACTISEAL catheters due to defects in sterile packaging that may compromise product sterility. The defect affects 106 units distributed worldwide.
Coviden Monoject 60ml Luer-Lock syringes were inadvertently distributed despite being quarantined. Mckesson Medical-Surgical is recalling approximately 100 units (lot 330737X) distributed in the United States.
Integra LifeSciences is recalling 135 CODMAN BACTISEAL EVD Catheter Sets due to defects in sterile packaging that may compromise product sterility.
The CORI Starter Kit surgical system may experience display flickering from a software tracking error, potentially causing surgical delays during orthopedic procedures.
Imprimis is recalling Klarity-C, a cyclosporine eye medication, because the company cannot assure the product meets sterility standards. Approximately 136,005 units were distributed nationwide.