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
PS Seasoning PSW21585 Save A Lot Bind 50# is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 992.5 lbs are affected.
Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Ghirardelli Chocolate Company is recalling certain lots of Premium Hot Cocoa Mix due to potential Salmonella contamination.
Ghirardelli Perfectly Premium Frappe Mix Chocolate Flavored, 50 oz, is being recalled over potential Salmonella contamination. 1,854 units are affected.
Solina Ranch Seasoning in 50 lb bags is being recalled because the product has the potential to be contaminated with Salmonella. 459 bags are affected.
Safecor Health, LLC is recalling Atomoxetine HCl 10 mg capsules because some units are incorrectly labeled as 10 mg when they actually contain 25 mg. Patients taking the mislabeled product may receive an incorrect dose.
Wisconsin Pharmacal Company is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant due to confirmed presence of Staphylococcus aureus contamination. Affected units are 6 oz tubes with Lot #1024088, expiring 11/30/2026, distributed nationwide and in the Bahamas.
Squirrel Brand Travelers Mix in 16 oz cans is being recalled over the potential presence of Salmonella. 3,858 cases are affected.
Ford is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles because the front seat belt pretensioner may inadvertently lock the belt so it cannot retract or extend.
VitaminAlly Liposomal Women's Liquid Multivitamin Drops with Iron are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
VitaminAlly Liposomal Mens 50+ Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Toyota is recalling certain Lexus UX Hybrid, Lexus GX, Toyota Mirai and Land Cruiser Hybrid vehicles because the instrument panel cluster may fail to display certain warnings or indicators.
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
Pure Libido Drink in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.
VitaminAlly Liposomal Collagen Booster is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
VitaminAlly Liposomal Womens 50+ Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Blackseed Bitters in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.
VitaminAlly Liposomal D3+B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal Sleep Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal Kids Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.
Ford is recalling certain 2021–2026 Bronco Sport and 2022–2026 Maverick vehicles due to potentially loose or improperly installed front lower control arm ball joints that could disconnect from the wheel knuckle, risking loss of vehicle control and crashes.