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.
Minimum severity
Hyundai is recalling certain 2026 Kona vehicles because the front steering knuckles may crack and break due to a manufacturing error, which can cause loss of steering control and increase crash risk.
Pending LLM rewrite. Source: NHTSA 25V102000.
Pending LLM rewrite. Source: NHTSA 26V070000.
Pending LLM rewrite. Source: NHTSA 24V051000.
Pending LLM rewrite. Source: NHTSA 24V054000.
Pending LLM rewrite. Source: NHTSA 24V052000.
Pending LLM rewrite. Source: NHTSA 24V053000.
Pending LLM rewrite. Source: USDA FSIS 007-2026.
MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.
Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.
Missry Associates recalls Misco Sports Light-Up Racket Sets (model MT2287) because the battery compartment screw can detach and button cell batteries in the shuttlecock can be easily accessed by children, posing risk of serious injury or death if swallowed.
Joy Furniture is recalling about 10,400 Talan and Royce sofas, loveseats, and recliners due to a fire hazard in the power switch that can overheat. The firm has reported 41 incidents including smoking, burning, and two fires, with no injuries reported so far.
Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.
Walmart is recalling about 165,000 Mainstays 9-Drawer Fabric Dressers because they can tip over and cause entrapment if not anchored to a wall, creating a risk of serious injury or death to children.
Giantex outdoor lounge chairs model NP10025NY pose an amputation risk when adjusting the backrest due to exposed pinch points. One finger amputation has been reported.
Daoen Inc. is recalling Zen Fidget Magnetic Ball Sets because the loose high-powered magnets can be swallowed by children, causing intestinal perforation, blockage, or death. No injuries have been reported.
Proudly American Store is recalling about 8,000 VL2020 lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Swallowed batteries can cause serious internal injuries and death.
Tzumi Electronics is recalling SLF Sauna Blankets that can overheat, posing fire and burn hazards. Six reports of overheating have been received, including five with minor property damage.
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
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.
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.