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.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Grundens recalled Youth Clipper 282 and Youth Zenith 282 jackets on October 30, 2025. Drawstrings in the hoods pose a strangulation risk for children. Consumers must stop using the jackets immediately and return them for refunds or credits.
DINBooonLUX recalled 12-inch full-size hybrid mattresses on October 30, 2025. The mattresses violate flammability standards, posing serious fire risks. Consumers should stop using the mattresses immediately.
YaFiti recalled its Fabric 12-Drawer Dressers on October 30, 2025, due to tip-over and entrapment risks. The dressers can pose serious injury or death risks, especially to children, if not anchored to the wall. Consumers should stop using the product immediately and return it for a full refund.
Kroger recalled Halloween-themed Skeleton Wax Candles on October 30, 2025. The candles contain flammable ornaments that pose fire and burn hazards. Consumers should stop using these candles and return them for a full refund.
Polaris Industries recalled certain 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 ROVs due to a fire hazard. The recall affects vehicles sold between March 2025 and August 2025. Polaris urges consumers to stop using the recalled vehicles immediately.
B Braun Medical recalled 12,700 IV administration sets on October 29, 2025, due to a risk of medication backflow. The affected models include Catalog Number 352062, distributed worldwide including the US, Canada, and Germany. Healthcare providers must stop using these devices immediately.
Medtronic recalled 6,591 extravascular implantable cardioverter defibrillators on October 29, 2025. The recall stems from a potential delay in high-voltage therapy that could occur under rare conditions. Patients must stop using the devices immediately and follow manufacturer instructions.
Medicrea recalled 44 units of its IB3D Universal Implant Inserter on October 29, 2025. The device's handle may untread from the shaft, preventing proper rotation of implants. The recall affects states including TN, CA, and TX.
B Braun Medical recalled 1,019 IV administration sets on October 29, 2025. The recall addresses a risk of medication backflow from secondary IV containers. Affected devices include catalog number 457506 and others.
B Braun Medical recalled 2,100 IV administration sets on October 29, 2025. The recall follows reports of backflow of medication from secondary IV containers into primary IV containers. This poses a high risk for patients using the Infusomat Space, Outlook, and Vista pumps.
B Braun Medical recalled IV Administration Sets on October 29, 2025, due to a backflow risk. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers should stop using the product immediately.
B Braun Medical recalled 19,392 anesthesia IV sets on October 29, 2025 due to the potential for medication backflow. The defective sets may cause occlusion and were sold worldwide, including in the US, Canada, Germany, Guatemala, and Singapore.
B Braun Medical recalled 10,536 Anesthesia IV Sets on October 29, 2025. The recall stems from a risk of medication backflow between IV containers. Healthcare providers must stop using the product immediately to prevent potential harm.
B Braun Medical recalled 32,500 IV extension sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled 23,160 IV administration sets on October 29, 2025. The sets pose a high risk of medication backflow from secondary containers into primary containers. Healthcare providers should stop using the devices immediately.
Philips North America recalled six units of the Incisive CT scanner on October 29, 2025, due to a serious safety hazard. The screws on the tube heat exchanger may not be properly tightened, leading to potential detachment during operation. This defect could cause damage to other components within the system.
Philips North America recalled 2,341 Incisive CT scanners on October 29, 2025. A component may detach and damage other parts during operation. Users must stop using the device immediately and follow recall instructions.
Avion Pharmaceuticals recalled 804 bottles of Prenate Chewable vitamins on October 29, 2025, due to undeclared soy. The recall affects consumers in 15 states, including California and Texas. The product also contains a labeling error regarding the amount of boron.
B Braun Medical recalled 7,008 IV administration sets on October 29, 2025. The recall stems from the potential backflow of medication from secondary IV containers. Healthcare providers and patients should stop using the devices immediately.
Medicrea recalled 44 units of its IB3D PL Instruments Set on October 29, 2025. The orthopedic rotation tool handle may untread from the shaft, causing it to fail during use. Healthcare providers and patients must stop using the device immediately.