Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
HOMEAL bed rails sold on Amazon are recalled after entrapment risk was identified. The recall applies to HOMEAL-branded children’s bed rails with Model No. 338. Consumers should stop using the product immediately and contact HOMEAL for a full refund.
Avenco and Novilla mattresses marketed by PT Champion are recalled for a serious fire risk. The recall covers models in 6, 10, 12 and 14 inches of thickness across twin to king sizes. Consumers should stop using these mattresses immediately and contact PT Champion for a free fitted cover or repair options.
Knog is recalling Blinder 900 and Blinder 1300 Front Bicycle Lights sold at multiple retailers. The recall covers units with batch codes printed on the underside. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Stop using the recalled lights and register for a free replacement at knog.com/recall.
Harppa recalled 5-in-1 convertible high chairs due to risk of serious injury or death from fall and entrapment hazards. The recall involves model BHC001 with production batch 202408. The chairs were sold in green, pink and gray. Consumers should stop using the product immediately and seek a replacement. Harppa provides a replacement option and destruction instructions for the recalled unit.
Crate & Barrel recalled Ana Dining Chairs sold at Crate & Barrel stores and Crateandbarrel.com from January 2021 through January 23, 2025 for a fall hazard. The chair legs can break, posing a fall risk. Stop using the recalled chair and contact Crate & Barrel to obtain a free replacement chair and arrange a free pickup.
Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.
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 33,528 Blood Administration Set units used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The sets have a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Health-care facilities should stop using the device immediately and follow the recall letter instructions.
B. Braun Medical recalled 150,664 Rate Flow IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices are cataloged as 375258. The recall addresses a potential backflow from piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s rec
B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.
Medtronic recalled 6,591 Aurora EV-ICD and Clinical EV-ICD single-chamber extravascular implantable defibrillators worldwide. A rare sequence of events could delay high-voltage therapy. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.
B Braun Medical recalled 162,648 Outlook IV Sets used with Infusomat Space Large Volume Pumps and related systems. The devices carry a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and patients should stop using the device immediately and follow recall instructions.
B. Braun Medical recalled 46,250 SAFELINE IV sets sold worldwide on Oct. 29, 2025. The devices pose a backflow risk from secondary piggyback IV containers into primary lines and may fail to prime due to occlusion. Hospitals and patients using Infusomat Space Large Volume Pump, Outlook Pump, or Vista Basic Pump with SAFELINE sets should stop use immediately and await manufacturer instructions.
B Braun Medical recalled 11,832 IV administration sets worldwide on Oct 29, 2025. The devices are used with Infusomat Space, Outlook, and Vista Basic Pumps. The hazard is backflow of medication and occlusion. Stop using the product immediately and follow manufacturer recall instructions. Check your model numbers and contact the manufacturer for refunds or replacements.
B. Braun Medical recalled 187,464 IV administration sets worldwide, including US distribution and shipments to Canada, Germany, Guatemala, and Singapore. The devices pose a backflow risk from secondary (piggyback) IV containers into primary containers and can fail to prime properly. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.
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.
B. Braun Medical recalled 49,330,370 Infusomat IV sets worldwide after a potential backflow from secondary to primary IV containers and an inability to prime. The recall covers gravity IV sets and pump sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Stop using any affected sets immediately and contact B. Braun Medical for instructions on refunds or replacement
B. Braun Medical Inc. is recalling 12,320 burette sets worldwide used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The device can allow backflow from secondary IV containers into primary containers and may fail to prime. Hospitals and clinics should stop using the device immediately and follow the recall instructions.
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.
B. Braun Medical recalls 7,008 IV administration sets sold worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow from secondary to primary IV containers and may fail to prime. Hospitals and patients should stop using the sets and follow the manufacturer’s recall instructions.