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
Boston Scientific is recalling EndoVive Replacement Button Kits due to sizing mislabeling that could cause undersizing and serious complications including tissue damage and sepsis.
3M recalled 764,580 Specialty Blade Assemblies for surgical clippers due to risk of burns from overheating. The blade can reach temperatures exceeding 77°C if left running improperly.
Abiomed is releasing software Version 8.5 for the Automated Impella Controller to fix an issue in versions 8.4 and 8.4.1 where the device failed to recognize the pump. Approximately 4,463 units were distributed nationwide.
Mennel Milling Company is recalling flour products due to potential contamination with metal, wood, gasket material, and sifter balls. Affected product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.
Canon Medical's INFX-8000F X-ray system may display abnormal horizontal stripe patterns due to a manufacturing change in the flat panel detector's internal board, potentially preventing exam completion.
Mennel Milling Company recalls Pizza 50/50 Unmalted flour due to potential metal, wood, gasket material, and sifter ball contamination. The affected product was distributed across KY, MI, NJ, NY, and PA.
Country Corner Dairy is recalling Sizzling Colby Cheese due to lack of proper pasteurization. The recalled product was distributed in Maryland and Virginia.
Mennel Milling Company is recalling 2.6 million pounds of bulk AP flour that may contain metal, wood, gasket material, and sifter balls. The flour was distributed in six states and should not be used.
M&P Production LTD is recalling raw lamb and beef samsa products because they contain sesame seeds, a known allergen, that are not declared on the label.
Isuzu is recalling certain FTR, FVR and Chevrolet LCF trucks with Mobileye Collision Warning Systems because a misrouted camera cable can damage wiring and overload the electrical circuit.
Philips Allura Xper fluoroscopic X-ray systems may experience memory module failures that cause the system to stop functioning and prevent imaging. This malfunction could delay critical medical procedures.
Mennel Milling Company is recalling approximately 2.6 million pounds of ALL PURPOSE EN EZ BL flour due to potential contamination with metal, wood, gasket material, and sifter balls.
Mennel Milling Company is recalling approximately 2.6 million pounds of PIZZA 50/50 UNMALTED flour due to potential contamination with metal, wood, gasket material, and sifter balls.
Mennel Milling Company recalled I-52 Patent Flour containing potential foreign material including metal, wood, gasket material, and sifter balls. The flour was distributed in bulk trailers across six states.
Mennel Milling Company is recalling its milling product (2-15969-0000) due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.
Philips is recalling 14 units of its Azurion 3 surgical imaging system due to a potential short circuit in the power inverter. The defect could cause the device to lose power and fail during surgical procedures.
Lupin Pharmaceuticals recalls Voriconazole for Oral Suspension (40mg/mL) due to missing or incorrect package inserts on affected batches distributed in Ohio, Illinois, and New Jersey.
W&H Surgical handpiece S-12 devices were incorrectly laser marked with '1:1' instead of the correct '1:2' during production. 160 units are affected.
Amneal Pharmaceuticals is recalling 46,037 bottles of Oseltamivir Phosphate Oral Suspension due to failed quality test results showing impurities and degradation. The FDA classified this as a Class II recall affecting nationwide distribution.
Meta Psyllium Fiber Capsules in 100 and 160 count bottles are being recalled because the product labeling is illegible. Approximately 21,428 cases were distributed across most US states.
Medline is recalling 1.3 million units of bleach germicidal wipes due to stability concerns. Products labeled for 24-month shelf life are only safe and effective for 12 months.
Mennel Milling Company is recalling approximately 2.6 million pounds of bulk milling product due to potential contamination with foreign materials including metal, wood, and gasket material distributed across six states.
Pure Care Foaming Mint Hand Sanitizer has been voluntarily recalled due to manufacturing process deviations. The product was distributed to accounts in North Carolina and Michigan.
Toyota is recalling certain 2022-2023 Tacoma trucks because the rear axle shaft may separate from the axle housing due to debris causing improperly secured fasteners, increasing the risk of a crash.
Nissan is recalling certain 2023-2024 vehicles, including the Rogue, due to a manufacturing issue that may allow the driver's air bag inflator to absorb moisture and deploy improperly.