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
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Blue Bird is recalling 2025-2027 Vision school buses because a missing support brace may cause the wheelchair lift to fail, increasing injury risk.
Philips North America is recalling the IntelliVue Patient Monitor MX850 over a potential issue where the monitors did not alarm.
Dreyer's Grand Ice Cream is recalling 3,410 cases of Haagen-Dazs mini chocolate dark chocolate ice cream bars over undeclared wheat.
Ventura Foods is recalling 700 cases of Publix Deli Carolina-Style Mustard BBQ Sauce after foreign objects, described as black plastic planting material, were found in granulated onion.
Great Lakes Cheese is recalling 1,900 cases of Happy Farms by Aldi Italian Style shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Philips North America is recalling the IntelliVue Multi-Measurement Module X3 over a potential issue where the monitors did not alarm.
Rong Shing Trading NY is recalling 10 cases of Aojia Dried Red Bayberry because the product contains undeclared sulfites at 7.39mg per serving, and cyclamates.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 4,131 cases of mozzarella and provolone shredded cheese blend, sold under four brands, over potential metal fragments from a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 3,397 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Enterix is recalling 201,426 InSure ONE Fecal Immunochemical Test kits after the test failed sensitivity testing with one test card lot, which may result in false negative results.
Avion Pharmaceuticals is recalling 804 bottles of Prenate Chewable after positive test results for soy, which is not listed on the label, and a boron amount stated in mg instead of mcg.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 4,298 cases of pizza style shredded cheese blend, sold under six brands, over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue MP5 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.