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
Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.
GreenGate Fresh Cello Spinach is being recalled due to potential E. coli (EHEC) contamination. The recall involves 11 cases distributed to eight consignees across seven U.S. states.
Le Croissant Tuna Salad (5.8oz) is recalled due to undeclared milk and soy allergens. Consumers with allergies to these allergens should not consume the product.
Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.
BMW is recalling certain 2023 models with a transmission control unit weld defect that may allow oil leakage, risking sudden power loss and increased crash risk.
Eltahan Inc. is recalling Eltahan Golden Raisins (400g, UPC 2337660022) distributed in NY, NJ, and PA due to undeclared sulfites, which can cause severe allergic reactions.
Terberg Benschop is recalling 2021-2022 YT193 terminal tractors because paint wear on the steering linkage may cause bolts to loosen or break, risking loss of steering control.
Textron Specialized Vehicles is recalling 2024 Cushman Hauler Pro LSVs because water may enter the battery module, damaging circuits and increasing fire risk.
Eldorado is recalling 2019-2023 Axess and EZR buses because a transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.
Gillig is recalling 3,626 Low Floor vehicles from 2021-2023 because an incorrect fuse in the rearview mirror system may overheat and cause a fire.
Mercedes-Benz is recalling 2,797 2024 GLE 450e vehicles because a software error may increase the distance required to stop, raising crash risk.
Pelleh Poultry Corp. is recalling approximately 708 pounds of ready-to-eat beef and poultry products due to possible Listeria monocytogenes contamination.
Spartan Fire is recalling 69 fire apparatus units from 2020-2023 because a firmware defect may cause electrical circuits to overheat and start a fire.
Peg Perego has recalled YPSI and Z4 inclined sleeper bassinets because they violate federal safety standards for infant sleep products and pose a risk of suffocation and falls.
Polaris is recalling about 2,900 Model Year 2022 Patriot 850 MATRYX snowmobiles because the ring gear on the primary clutch can fail, causing clutch components to come loose and creating an injury hazard. Nine failures have been reported, including one injury.
Unomedical recalls 3,362 units of VariSoft infusion sets due to connector damage causing premature disconnection and missed insulin doses, risking dangerous elevation of blood glucose and ketone levels.
FDA recalls Polyvinyl Alcohol 1.4% Lubricating Eye Drops nationwide due to non-sterile manufacturing conditions found during inspection.
Cardinal Health is recalling LEADER brand Eye Irritation Relief drops due to non-sterility concerns. FDA testing found insanitary conditions and positive bacterial results at the manufacturing facility, affecting 11,629 units distributed nationwide.
Cardinal Health is recalling all lots of LEADER brand Dry Eye Relief nationwide due to non-sterility. FDA found insanitary manufacturing conditions and positive bacterial test results.
Unomedical is recalling 8,028 VariSoft infusion sets due to a manufacturing defect that makes the connector prone to unintended disconnection, potentially leading to missed insulin doses and serious blood glucose complications.
Cardinal Health is recalling all lots of LEADER brand Lubricant Eye Drops due to non-sterility issues. FDA found insanitary conditions and positive bacterial test results at the manufacturing facility in India.
Cardinal Health is recalling all lots of LEADER brand Lubricant Eye Drops nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results from the manufacturing facility.
The FDA recalls 1,679 VariSoft infusion sets (Model 1002828) due to connector damage that causes improper detachment. Undetected disconnections can lead to missed insulin doses and diabetic ketoacidosis.
LEADER brand Lubricant Eye Drops are being recalled nationwide due to non-sterility issues. FDA testing found insanitary conditions and positive bacterial contamination at the manufacturing facility.
Rugby Laboratories' Lubricating Tears Eye Drops are being recalled nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results at the manufacturing facility.