1,716 recalls tagged with “cpsc regulated”.
Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.
R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.
BBWOO recalled baby loungers on January 15, 2026, due to serious injury risks. The loungers violated safety standards, posing entrapment and fall hazards. Consumers should stop using the product immediately and seek a refund.
Curtis International recalled 50,000 Frigidaire-brand minifridges on January 15, 2026, due to fire and burn hazards. The recall affects model EFMIS121 and previously recalled models EFMIS129, EFMIS137, EFMIS149, and EFMIS175. Consumers should stop using these minifridges immediately and seek a refund.
Energizer recalled its Large Power Indicator Lantern on January 15, 2026. The recall affects models with a date code of June 2024. Overheating lithium-ion batteries pose a burn risk to consumers.
Live it Up brand recalled 795,834 units of Super Greens powder on January 15, 2026, due to possible Salmonella Typhimurium contamination. The affected products are sold nationwide, including Puerto Rico and Guam. Consumers should not consume the product and seek refunds immediately.
Superfoods, Inc. recalled 795,834 units of Live it Up brand Super Greens on January 15, 2026. The dietary supplement may be contaminated with Salmonella Typhimurium, posing a health risk. Consumers should stop using the product immediately and seek a refund or replacement.
WinCo Foods recalled 5,066 cases of Deli Margherita Pizza on January 15, 2026, due to potential metal fragments. The affected item is a 17oz Take & Bake pizza. Consumers should not consume the product and seek refunds immediately.
Aonic Inc. recalled 3,630 bottles of Aonic Complete Hers dietary supplement on January 15, 2026. Possible contamination with coliforms, E. coli, and Pseudomonas aeruginosa prompted the recall. Consumers in Utah should stop using the product immediately.
Aonic Inc. recalled 780 bottles of its Complete dietary supplement on January 15, 2026, due to potential contamination with E. coli and Pseudomonas aeruginosa. Consumers in Utah should stop using the product immediately and seek refunds or replacements. The recall affects specific lots with expiration dates of December 27, 2026.
LUBNA QUALITY PRODUCTS recalled 400 cases of mung beans on January 15, 2026, due to the presence of Thiamethoxam, a pesticide. The affected products were distributed in Texas and Louisiana. Consumers should not consume the product and should seek refunds or replacements.
Encore Medical, LP recalled 14 EMPOWR 3D Knee implants on January 15, 2026. The implants contain incorrect labeling that poses a risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.
Rose and Shore recalled 5,067.1 cases of 14" Margarita Thin Crust Pizza sold at a single regional chain in California, Oregon, Arizona, Idaho and Texas. A potential foreign object has been found in tomatoes used in the product. Consumers should not eat this pizza and should contact Rose and Shore for refund or replacement by email.
Sevillo Fine Foods recalled 2,372 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina. The product may contain metal fragments. Consumers should not consume the product and should contact Sevillo Fine Foods for refunds or replacements.
KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.
Organic Spices, Inc. recalled 6,288 jars of garlic salt on January 14, 2026. The product contains salt, which is not listed on the label. The recall impacts several states including California and New York.
Edermy LLC recalled 11,202 medical devices on January 14, 2026. The recall affects models P2HC-A, P2HC-S, and P2HC due to lack of proper FDA clearance. Patients and healthcare providers should immediately cease use of these devices and follow recall instructions.
Edermy LLC recalled the PIE Trolley System Model 2005 on January 14, 2026 due to a lack of 510K clearance. The recall affects 27 units distributed nationwide across 15 states. Users must stop using the device and follow the manufacturer's instructions immediately.
Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.
Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.