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
About 3,090 Meaicezli Play Purse Sets are being recalled because the toy cell phone contains button cell batteries and the toy tablet a lithium coin battery that children can easily access.
About 4,740 KKL Fabric 9-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
About 1,040 TopHomer 8-inch pool drain covers are being recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act.
About 16,800 Furnulem 8-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the mandatory standard required by the STURDY Act.
International Motors is recalling 2026-2027 IC Bus CESB school buses because wheelchair retractors may not lock, increasing injury risk.
Ford is recalling certain 2025 and 2026 Maverick vehicles because the instrument panel cover may separate during an airbag deployment, potentially striking occupants and increasing injury risk.
Ford is recalling 2022 Transit vehicles where the rearview camera may display a blank image, increasing the risk of a crash while reversing.
About 12,000 JOKOSIS portable bed rails, model HC0262, are being recalled because users can become entrapped within the rail or between the rail and the mattress.
General Motors is recalling 2025–2026 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not produce sufficient volume change between stopped and low-speed operation, failing to meet federal safety standards.
Honda is recalling 2024–2026 CBR600RR motorcycles because the cylinder head may have been improperly manufactured, risking rear wheel lockup and engine fire.
Altec is recalling certain 2023-2025 Aerial Device and Digger Derrick vehicles because the electronic taillight module harness may have inadequate circuit protection.
About 260 Currey & Company Electra chandeliers are being recalled because the component connecting the fixture to the ceiling mount is not threaded properly and the fixture can fall.
Chetak New York is recalling Deep-brand frozen arvi after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen tuvar lilva after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Draeger is recalling 118,850 ErgoStar CM 55 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen guvar after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Draeger is recalling 2,050 ErgoStar CM 60 airway connectors after multiple complaints in which cracks formed in the hose of specific catheter mounts. The FDA has classified the action as Class I.
Moonlight Packing is recalling 439 bags of 4-count Peppermint Peach packs over potential contamination with Listeria monocytogenes. The FDA has classified the action as Class I.
Moonlight Packing is recalling a further 2,622 cases of loose bulk peppermint peaches over potential Listeria monocytogenes contamination, under enforcement record H-0324-2026.
Chetak New York is recalling Deep-brand frozen mixed vegetables after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen red pearl onions after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen green chili cubes after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen aviyal mix after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Chetak New York is recalling Deep-brand frozen tindora after the product tested positive for Salmonella. The FDA has classified the action as Class I.
Moonlight Packing is recalling 2,603 cases of loose bulk peppermint peaches over potential contamination with Listeria monocytogenes, under enforcement record H-0323-2026.