Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
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.
Crate & Barrel recalled Ana Dining Chairs on October 30, 2025, after reports of leg failures. The chairs pose a fall hazard, affecting models sold from January 2021 to January 2025. Consumers should stop using these chairs immediately and contact the company for a replacement.
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.
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.
Knog recalled the Blinder 900 and Blinder 1300 Front Bicycle Lights on October 30, 2025, due to fire hazards. The lithium-ion batteries can overheat and ignite, presenting a serious risk to users.
HOMEAL recalled portable bed rails on October 30, 2025, after identifying a serious entrapment risk. The bed rails violate safety standards, posing a risk of injury or death to children. Consumers must stop using the product and contact the manufacturer for a full refund.
H-E-B recalled 12-pack Destination Holiday Glow Light Stick bracelets due to a skin irritation hazard. The affected bracelets were sold in multiple colors and can leak. Consumers should stop using the product immediately and seek a refund.
Milwaukee Tool recalled M18 FUEL Top Handle Chainsaws due to a laceration hazard. The recall affects approximately 10,000 chainsaws sold since January 2023. Consumers should stop using the product immediately and contact Milwaukee Tool for a free repair.
Olympus Corporation of the Americas recalled 7,803 units of the HX-400U-30 ligating device on October 30, 2025. The device may fail to release as intended, posing significant risks to patients. Healthcare providers must stop using the device immediately and follow recall instructions.
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.
B Braun Medical recalled 3,120 IV administration sets on October 29, 2025, due to a risk of medication backflow. The recall affects models used with Infusomat Space, Outlook, and Vista Basic Pumps. The company advises patients and healthcare providers to stop using the devices immediately.
B Braun Medical recalled 74,652 IV administration sets on October 29, 2025. The recall impacts users of the Infusomat Space, Outlook, and Vista Basic Pumps due to backflow risks. The affected catalog number is US9923F, with worldwide distribution including the US and Canada.
B Braun Medical recalled 65,904 IV administration sets on October 29, 2025, due to a risk of backflow from secondary IV containers. This could lead to medication errors that may endanger patients. The sets are used with several pumps, including the Infusomat Space and Outlook Pump.
B Braun Medical recalled 104,784 Anesthesia IV Sets on October 29, 2025. The recall affects models utilized with Infusomat Space, Outlook, and Vista pumps due to potential medication backflow. This hazard poses serious risks for patients receiving IV medication.
B Braun Medical recalled 28,344 IV administration sets on October 29, 2025. The recall affects gravity and pump administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. Users face a high risk of medication backflow into primary IV containers.
B Braun Medical recalled 129,480 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary containers. Patients and healthcare providers must stop using the devices immediately.
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 over 20 million IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication that could put patients at risk. Healthcare providers and patients must stop using the devices immediately.
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.