These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
1,498 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Mylan Institutional LLC recalled 800 vials of Haloperidol Lactate Injection on October 10, 2025, due to incorrect RFID tag labels. The product may pose a risk due to potential mislabeling affecting tracking and administration. Healthcare providers should stop using the product immediately and follow up with Safecor Health for guidance.
EcoFlow Technology recalled Delta Max 2000 Power Stations due to a fire hazard. The recall affects model EFD310, identified by a black and silver design. Consumers should stop using the product immediately and seek a firmware update for repair.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
STAQ Pharma Inc. recalled Hydromorphone HCL PF injections on October 9, 2025, due to incorrect or missing lot and expiration dates. The recall affects products distributed nationwide across the U.S. Healthcare providers and consumers must immediately cease using the affected medication.
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.
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.
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.
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.
Glycar SA Pty. recalled 18 units of the SJM Pericardial Patch on October 9, 2025. The affected lot may not meet required tensile strength specifications. Healthcare providers and patients should stop using this device immediately.
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.
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.