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
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.
Nutrition for Longevity is recalling 635 Loaded Veggie Grain Bowls shipped directly to consumers over potential contamination with Listeria monocytogenes.
Philips North America is recalling the IntelliVue Patient Monitor MX750 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 Multi Measurement Server X2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Hale inc is recalling 54 bottles of Lotsa Pasta Fresh Basil Infused Olive Oil over the potential for Clostridium botulinum contamination.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Blonde Beard's is recalling 4,888 8 oz bottles of Dojo Asian Wing Sauce because the product contains undeclared soy.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
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.
Great Lakes Cheese is recalling 15,490 cases of Italian style shredded cheese blend, sold under eight 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.
Pacific Seafood is recalling 15,498 lbs of Raw Blackened Shrimp because the shrimp may contain 3.4mg sulfur dioxide per serving and the label does not declare sulfite.
Prime Food Processing is recalling frozen Lava Bun with Green Tea Flavor because the products do not declare milk in the Contains statement or the ingredient statement.
Dreyer's Grand Ice Cream is recalling 3,410 cases of Haagen-Dazs mini chocolate dark chocolate ice cream bars over undeclared wheat.
Great Lakes Cheese is recalling 117 cases of Food Club Finely Shredded Pizza Style Four Cheese Blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue MP30 over a potential issue where the monitors did not alarm.
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.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.