Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
STAQ Pharma Inc. recalled FentaNYL Citrate PF on October 9, 2025, due to incorrect or missing lot and expiration dates. The injection, distributed nationwide, poses a high hazard risk. Consumers and healthcare providers should stop using the product immediately.
YGJT recalled baby loungers on October 9, 2025, due to risks of serious injury or death. The loungers violate safety standards, posing dangers of entrapment and falls. Consumers should stop using these products immediately and seek refunds.
Pivotal Health Solutions recalled 34 heated massage tables on October 9, 2025. The heat function may overheat, posing a risk of smoldering and melting. Affected units are distributed nationwide in the U.S., Canada, and Japan.
American Health Packaging recalled 27,868 blister packs of Sucralfate Tablets on October 9, 2025. The company filed for Chapter 11 bankruptcy, impairing its ability to monitor product quality. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Bmrwtg recalled LED tutu skirts on October 9, 2025, due to a serious risk of battery ingestion. The skirts, sold in multiple colors, can expose children to dangerous lithium coin batteries. Parents should stop using these products immediately and follow recall instructions.
Calico Brands recalled Scripto Premium Torches on October 9, 2025. The torches pose a high risk of fire and burn injuries due to safety standard violations. Consumers should stop using the product immediately and seek a refund.
Ritons recalled Generic magnetic ball sets on October 9, 2025. These toys pose a serious risk of injury or death from magnet ingestion. Consumers should stop using these products immediately and follow the recall instructions.
Rong Shing Trading NY Inc recalled Aojia Dried Red Bayberry on October 9, 2025. The product contains undeclared sulfites and cyclamates, posing a risk to consumers. Ten cases were distributed in Virginia, New Jersey, Massachusetts, and New York.
Waymeet expanded its recall of ESR HaloLock wireless power banks on October 9, 2025. The models 2G505, 2G520, 2G505B, and 2G512B pose serious burn and fire hazards. Consumers must stop using these devices immediately and return them for a full refund.
USV Private recalled 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution on October 9, 2025. The solution exceeded impurity specifications, posing a health risk. Consumers should stop using the product immediately and contact their healthcare provider.
STAQ Pharma Inc. recalled Ketamine Hydrochloride 50mg/5 mL syringes on October 9, 2025. The recall affects products with incorrect or missing lot and expiration dates. The FDA classified this recall as Class III due to potential risks to patient safety.
Guangzhou Jiguang Lighting recalled 50,000 Living Glow portable waist fans on October 9, 2025. The lithium-ion batteries can overheat while charging, posing a high fire hazard. Consumers should stop using the fans and seek a refund immediately.
Mom Genius recalled Retractable Safety Gates on October 9, 2025, due to a risk of serious injury or death. The gates violate mandatory safety standards and pose an entrapment hazard. Consumers should stop using the gates immediately and seek a refund.
Taoscare recalled 3 boxes of motion sickness patches on October 9, 2025. The product was marketed without an approved NDA/ANDA. Consumers should stop using the patches immediately and seek guidance.
Bellabu Bear recalled its collection of children's robes on October 9, 2025. The robes violate flammability standards, posing a burn risk. Consumers should stop using the robes immediately and seek a refund.
Tempo USA recalled all Ambiano electric pressure cookers on October 9, 2025, after multiple burn injuries were reported. The recalled models include 93550 (KY-318B), 96775 (KY-318A), and 98527 (6L-PC). Consumers should stop using these pressure cookers immediately and seek a refund.
C-RAD POSITIONING AB recalled 189 Catalyst and Catalyst+ devices on October 9, 2025, due to issues with stereotactic radiosurgery (SRS) treatment. The defect may lead to incorrect patient positioning, potentially compromising treatment effectiveness. The recall affects devices distributed across 37 countries, including the United States.
Sprouts Farmers Market recalled 4,896 units of Smoked Mozzarella Pasta Salad on October 8, 2025. The salad may contain Listeria monocytogenes, a serious pathogen. Consumers should not eat the product and seek refunds immediately.
AstraZeneca recalled 916 pre-filled syringes of Fasenra on October 8, 2025. The recall follows a lack of assurance of sterility, posing serious health risks. Consumers and healthcare providers must stop using the product immediately.
Rising Pharma Holdings recalled 2,064 bottles of Carbidopa, Levodopa, Entacapone tablets on October 7, 2025. The recall followed reports that bottles contained incorrect dosages. The affected product poses a high risk due to potential overdose.