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
Jack & the Green Sprouts Alfalfa & Onion is being recalled due to potential Listeria monocytogenes contamination. Affected lot 300 with expiration date 10/9/24 should be discarded.
Dakota Toms Pepperjack Cheese Burgers are recalled for potential Listeria monocytogenes contamination. Affected products expire between 9/1/24 and 11/28/24.
Wismettac Asian Foods recalls Shirakiku Korean Seasoned Seaweed due to incorrect product labeling that fails to disclose sesame. Affected products were distributed in CA, AZ, TX, NM, WA, NY, and NV.
Dakota Tom's The Gambler sandwiches are recalled for potential Listeria monocytogenes contamination. Products were distributed to retail locations in ND, SD, WY, IA, and MN, with expiration dates September 1–November 28, 2024.
Jack & the Green Sprouts Alfalfa sprouts (5 oz containers) are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Iowa, Minnesota, and Wisconsin.
Reser's Fine Foods is recalling Ginger Chicken Broccoli Salad Kit V due to potential Listeria monocytogenes contamination in the cooked chicken. The product was distributed to 31 states.
Enoki mushroom packages distributed across seven states are being recalled due to Listeria monocytogenes contamination. Consumers should not consume the affected product and should return it to the point of purchase.
Maquet Cardiovascular is recalling the VasoView HemoPro Endoscopic Vessel Harvesting System due to silicone detachment from the Harvesting Tool Jaws during use. This FDA Class I recall affects 28,809 units worldwide.
PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.
Integra LifeSciences is recalling surgical patties and strips (Model 801452) due to higher-than-expected endotoxin levels in raw materials that may result in out-of-specification contamination. Approximately 4,818 units are affected.
The AVOXimeter 1000E blood oximeter (Serial Number 6824) has calibration values that are higher than normal, causing false oxygen level readings. This may lead to patient care mismanagement based on inaccurate data.
Codman Surgical Patties and Strips are being recalled due to higher-than-expected endotoxin levels in raw materials. Approximately 93,782 units were distributed worldwide for use in protecting tissue during surgery.
Integra LifeSciences is recalling surgical patties and strips (Model 801409) used in surgery due to higher-than-expected endotoxin levels detected in raw materials. No illnesses have been reported.
Integra LifeSciences is recalling surgical patties and strips (Model 801451) worldwide due to higher-than-expected endotoxin levels in raw materials that may result in out-of-specification contamination.
Abbott is recalling 13,318 units of its Alinity m HPV AMP Kit due to iron leaching into the lysis solution, causing positive controls to fail and potentially producing false negative test results.
Integra LifeSciences Corp. is recalling 128 units of Duraform Dural Graft Implant (Model 80-1477US, Lot CT007694) due to endotoxin levels exceeding specifications. No adverse events have been reported.
Dr. Reddy's Laboratories is recalling Cinacalcet 90 mg tablets due to N-nitroso impurity exceeding FDA limits. Patients should contact their healthcare provider.
Beckman Coulter is recalling over 465,000 thyroglobulin antibody test kits because their instructions incorrectly state that biotin interference was addressed. The false information could lead to false-low test results.
Reser's Fine Foods is recalling 420 cases of Asian Style Stir Fry meal kits containing potentially contaminated cooked chicken due to Listeria monocytogenes. Affected products were distributed across 30 states with Use By dates from September through November 2024.
BLI International is recalling Chlorpheniramine Maleate 4 mg tablets because the product failed stability testing, showing increased potency beyond specified limits. The recall affects 4,901 cases distributed to customers in Ohio and Missouri.
Reser's Fine Foods is recalling Don Pancho Chicken Quesadilla Express Meal Kits due to potential Listeria monocytogenes contamination in the cooked chicken component. No illnesses have been reported.
Integra LifeSciences is recalling Surgical Patties and Strips (Model 801457) due to higher-than-expected endotoxin levels in raw materials. These surgical devices protect tissue during operations, including brain and nervous system procedures.
Reser's Fine Foods is recalling Bistro 28 Creamy Green Chile Chicken Enchilada Meal Kits due to Listeria monocytogenes contamination in the cooked chicken. The affected meal kits were distributed across 30 U.S. states.
Nihon Kohden America is recalling its Adult/Pediatric Forehead Disposable SpO2 Sensor (Model 809030006) because the device was distributed without FDA market approval or clearance.
King Systems Corp. is recalling AMBU King LTSD oropharyngeal airways because they were marketed for pediatric use without FDA clearance for that indication. The device exceeded its 510(k) exemption limitations.