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
Kingdom Honey Royal Honey VIP is recalled due to undeclared sildenafil, a pharmaceutical ingredient. The product was distributed nationwide; all lots are affected.
North American Diagnostics is recalling SARS-CoV-2 rapid antigen test kits that were distributed without FDA approval or clearance. Approximately 122,366 units were sold to consumers across multiple US states and internationally.
The FDA has recalled Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder due to undeclared Tadalafil. The product was distributed in seven states and poses serious health risks.
Matzim LA Extended-Release Tablets, 240 mg are being recalled due to failed dissolution specifications. Patients taking this medication should consult their doctor about their treatment.
The FDA is recalling 399 units of the PRESTIGE RETRACTION GRASPER surgical instrument due to risk of weld separation between the handle and shaft. This defect could cause device malfunction during surgical procedures.
St. Jude Medical recalled Merlin 2 PCS MER3400 programmer software version 1.1.2 revision 1 or earlier in an FDA Class II recall. The recall affects 622 units distributed across the United States and internationally.
Navistar is recalling 2023 International and IC Bus commercial vehicles because the engine control module may short-circuit, causing the engine to stall unexpectedly. This defect increases the risk of crashes.
Refrigerated dressings sold under Cindy's and Bolthouse brands from United Natural Foods, Inc. are being recalled due to temperature abuse during delivery to stores in Alabama and Mississippi.
United Natural Foods, Inc. is recalling multiple brands of frozen vegetable products distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.
Food trailers experienced temperature control failures while transporting frozen food products to retail stores in Alabama and Mississippi. The products experienced temperature abuse that could affect food safety.
St. Jude Medical's Merlin PCS 3650 programmer software may display overestimated predicted battery longevity for certain pacemakers. This could affect clinical decision-making regarding device maintenance and replacement timing.
Neotract Inc is recalling 18,722 UroLift Systems due to potential improper implant deployment during use. Patients should contact their healthcare provider.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Combo Pack because the acidified/low acid dietary supplement was manufactured without an FDA-approved process.
Dental Choice is recalling 708 units of the CustMbite Model CBT-SRS-UL device nationwide because it was marketed and sold without FDA clearance.
Natural Grocers Amaranth Grain has been recalled due to potential Salmonella contamination. The FDA Class II recall affects 6,351 units distributed across 21 states.
Ragozzino Foods is recalling Creamy Parmesan Risotto distributed in New York, Florida, Illinois, and California due to potential glass contamination. Consumers should not eat the affected product.
Thor Motor Coach is recalling 2022-2023 motorhomes whose electric retractable awning may drop due to a failing welded seam. This increases the risk of injury.
Intuitive Surgical is recalling 505 E-100 electrosurgical generators because required preventative maintenance was not performed on units distributed worldwide and in the US.
St. Jude Medical recalls Merlin 2 PCS model MER3700, software used to program and interrogate Abbott implantable medical devices.
United Natural Foods, Inc. is recalling multiple brands of frozen prepared foods distributed to retail stores in Alabama and Mississippi due to temperature abuse during delivery. The temperature-abused foods may have been exposed to unsafe conditions allowing bacterial growth.
Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.
United Natural Foods, Inc. recalls frozen deli salads and prepared foods distributed in Alabama and Mississippi due to temperature abuse during delivery to retail stores.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Nighttime due to manufacturing without an approved acidification process. The product's preservation safety cannot be assured.
Multiple frozen seafood products from various brands distributed in Alabama and Mississippi were recalled due to temperature abuse during delivery to retail stores. No illnesses have been reported.
United Natural Foods, Inc. is recalling Grandpa's brand yogurt muffins sold in Alabama and Mississippi due to temperature abuse during delivery to retail stores. No illnesses have been reported.