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
EarthRoamer is recalling 2022-2023 LTi motorhomes because a control module may cause fuel to overflow and leak, increasing fire risk.
Braun Ambulances is recalling 2023-2024 models because a lighting control module defect may cause turn signals, brake lights, and backup alarms to fail, increasing crash risk.
Lolanta children's hooded flannel bathrobes violate federal flammability regulations for children's sleepwear and pose a burn hazard. About 16,900 units were sold online from January 2021 through October 2023.
Ford is recalling certain 2023 Explorer vehicles with a loose or missing fastener in the front suspension. This can cause steering pull and brake failure, increasing crash risk.
USDA FSIS issued a public health alert for ready-to-eat poultry products containing dairy recalled for possible Listeria monocytogenes contamination.
VPR Brands is recalling about 62,200 disposable lighters (Slim Soft and Slim Jet models) sold between September 2022 and November 2023 because they lack child-resistant mechanisms required by federal regulation, posing fire and burn hazards to young children under 5.
Denver Solutions is recalling 29,016 Phenylephrine HCl IV bags distributed nationwide. A filling system malfunction can result in some bags receiving double doses of this potent injectable drug.
Fat Choy Kee Dried Longan produced by HY SUCCESS INC. is being recalled because it contains undeclared sulfites. Sulfites are a known allergen that poses health risks to sensitive individuals.
Denver Solutions is recalling 7,548 IV bags of vancomycin due to a manufacturing system malfunction that can deliver double doses. The product was distributed nationwide.
The FDA has recalled Zenzedi (Dextroamphetamine Sulfate) 30 mg tablets due to a labeling error. The recall affects 4,662 bottles distributed nationwide.
GE HealthCare is recalling EvAir compressor kits for CARESCAPE and Engström ventilators due to elevated formaldehyde levels found in preliminary testing. The recall affects 1,294 units distributed worldwide.
Denver Solutions recalled 8,976 IV bags of fentanyl citrate nationwide due to a malfunction in the semi-automated filling system that could deliver double the intended dose.
Suzuki is recalling 2024 GSX-8R motorcycles because the drive chain may detach due to missing rivets, which can cause a loss of power to the rear wheels and increase crash risk.
FDA recalls EVair 03 air compressors (models 1609000, 1609002) for elevated formaldehyde when used with certain ventilators. The hazard was identified during preliminary testing under worst-case conditions: elevated room temperature (40°C) and minimal gas flow (2 L/min).
Rizo Lopez Foods has recalled multiple sour cream and cream products due to Listeria monocytogenes contamination. Products were distributed across multiple U.S. states.
Tio Francisco Yogurt products in multiple flavors are being recalled due to potential Listeria monocytogenes contamination. Consumers who have purchased these yogurts should not consume them.
EVair air compressors (models M1230849, M1230847) made by Datex-Ohmeda are being recalled after testing detected elevated formaldehyde emissions. The compressors are used with CARESCAPE R860 and Engström ventilator systems.
Denver Solutions is recalling 10,152 Vancomycin IV bags nationwide because a filling system malfunction can deliver double doses of the antibiotic medication.
Rizo Lopez Foods is recalling Tio Francisco Queso Seco 14 oz. cheese due to Listeria monocytogenes contamination. The product was distributed across multiple U.S. states with production dates through July 31, 2024.
Olympus recalls EZDilate Wire Guided Balloon devices used for endoscopic dilation due to reported bursting, leaking, and retrieval failures affecting 1,639 units nationwide.
Olympus is recalling 2,991 EZDilate endoscopic balloons for problems with inflation and deflation. Reports include device bursting and leaking, and retained foreign bodies in patients during procedures.
Rizo Lopez Foods recalled Oaxaca cheese products sold under multiple brand names due to potential Listeria monocytogenes contamination. The recall affects products distributed across multiple U.S. states.
Olympus is recalling approximately 6,898 EZDilate Wire Guided Balloon devices due to reported bursting, leaking, and retrieval problems during medical procedures.
Olympus recalled 3,354 EZDilate wire-guided dilation balloons due to failures in inflation, deflation, and retrieval, with incidents of bursting, leaking, and foreign bodies left in patients.
Rizo Lopez Foods, Inc. is recalling various queso fresco products from multiple brands due to potential Listeria monocytogenes contamination. The affected products were distributed to retail locations in multiple U.S. states.