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
Patoolio Direct pressure washers sold on Amazon lack a ground-fault circuit-interrupter (GFCI), creating serious electrocution and shock risk. Consumers should stop using them and contact the company for a refund.
SpringFlower 5-in-1 Montessori Toy Sets contain an airplane-shaped teething toy with tentacles that pose a choking hazard to young children. No injuries have been reported.
Apex Gaming PCs is recalling about 17,730 Manik and Apex-branded ATX computer power supplies sold online from December 2021 through February 2026 due to missing electrical hazard warning labels. Units lack proper warnings about shock and electrocution risks if opened.
The Sanlebi Pet Vet Playset is recalled because button cell batteries in the nail grinder and otoscope can be easily accessed by children. Consumers should immediately remove these components and contact Letokids for a refund or replacement.
Fengrong Tool electric pressure washers lack integral GFCI protection, posing serious electrocution risk. About 500 units sold via Amazon from October 2025 through January 2026 for $80–$130. Consumers should stop using immediately and contact Fengrong Tool for refunds.
ZOLIQUEX adult portable bed rails sold on Amazon from August 2023 through February 2026 violate federal safety standards due to entrapment hazards that could cause asphyxiation. About 16,000 units were affected.
Macy's is recalling Arch Studio tea kettles because the handle can detach during use when heated, posing a risk of burn injury. About 4,600 kettles were sold nationwide from August 2025 through February 2026.
ZMC Group is recalling LED Finger Beam Lights because the toy contains easily accessible button cell batteries that children can swallow, risking serious internal chemical burns or death.
BAYOTAK USA electric pressure washers lack a ground-fault circuit-interrupter (GFCI), creating a serious shock and electrocution hazard. No injuries reported. Consumers should stop using the product and contact the importer for a free replacement.
Agiiman Electric Pressure Washers lack ground-fault circuit-interrupter (GFCI) protection, creating a serious risk of electrical shock and electrocution. Consumers should stop using these units immediately and contact Agiiman for a full refund.
Lil' Buddies Pet Laser Toys are recalled by JC Sales for battery ingestion hazard from button cell batteries. About 51,160 units sold from February 2023–November 2025; no injuries reported.
ATOYUS Children's Activity Cubes are recalled for choking and small parts hazards affecting children under 3. About 70 units were sold on Amazon between January and February 2026.
Certain Generac portable generators may leak fuel from the carburetor when first filled with gasoline, creating a risk of fire or burn injury. About 149,400 units are affected.
Medline is recalling 439 medical convenience kits worldwide containing defective NAMIC Angiographic RA Control Syringes. The syringe rotating adaptor may unwind during use, causing loose or full disconnection between the syringe and manifold.
Medline's NAMIC Angiographic Control Syringes are being recalled because the rotating adaptor may unwind during use, potentially causing disconnection from the manifold. This Class I recall affects 192,690 units distributed worldwide.
The FDA recalled Red Bull Extreme Male Enhancement Supplement distributed in New Jersey due to undeclared sildenafil. The product contains an unlabeled prescription drug ingredient that poses health risks from drug interactions and contraindications.
Blue Bull Extreme Male Enhancement Supplement has been recalled due to undeclared sildenafil, a prescription pharmaceutical ingredient. The product was distributed in New Jersey.
NAMIC Angiographic Syringes may have rotating adaptors that unwind during use, causing loose or complete disconnection from the manifold, affecting 2.6 million units distributed worldwide.
Medline Industries is recalling 1,698 medical convenience kits containing angiographic syringe adaptors that may unwind during use, causing loose or disconnected connections between components.
Medline is recalling angiographic syringes because the rotating adapter may unwind during use, causing loose or complete disconnection between the syringe and manifold.
Medline recalled 966 medical convenience kits containing NAMIC control syringes because the syringe rotating adaptor may unwind during use, causing loose or complete disconnection from the manifold.
Medline medical convenience kits containing NAMIC syringe adaptors may unwind during use, causing loose or disconnected connections. Affected kits have been distributed worldwide.
Medline is recalling NAMIC Angiographic Syringes because the rotating adaptor may unwind during use, causing loose or full disconnection from the manifold. The FDA classified this as a Class I recall.
Medline is recalling medical procedure kits because the syringe rotating adaptor may unwind during use, potentially causing disconnection between the syringe and manifold.
Medline recalls 3,120 medical convenience kits containing control syringes due to a potential risk that the rotating adaptor could unwind during use, causing loose or complete disconnection from the manifold.