269 recalls tagged with “metal”.
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.
WLIVE expanded its recall to include 16-drawer fabric dressers sold on Amazon. The hazard is tip-over and entrapment risk that can cause serious injury or death to children. Stop using the recalled dressers immediately if not anchored to a wall and contact WLIVE for a full refund.
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.
HEB recalls a 12-pack Destination Holiday Glow Light Stick Bracelets sold in Texas after the green bracelet can leak and irritate skin. The recall involves bracelets in green, red, pink, orange, yellow and blue colors with UPC 9787014483. Consumers should stop using the green bracelet immediately and return the 12-pack to H-E-B for a full refund.
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.
B Braun Medical recalled 41,976 IV Administration Sets sold worldwide after identifying a backflow risk. The device can allow medication to flow from secondary (piggyback) containers into the primary IV line and may not prime properly. Hospitals and healthcare providers should stop using the sets immediately and await recall instructions from B Braun Medical.
B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.
B. Braun Medical recalled 122,232 IV administration sets sold worldwide through multiple medical distributors. The devices have a backflow risk from secondary (piggyback) IV containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the sets and follow the manufacturer's 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 7,344 Blood Administration Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may allow backflow from secondary (piggyback) IV containers into primary IV containers and cannot be primed. Hospitals and healthcare providers should stop using the devices immediately and follow manufacturer instructions.
B Braun Medical recalled 24,624 Blood Administration Sets worldwide. The recall covers sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The risk involves backflow from secondary IV containers into primary containers and the inability to prime. Hospitals and clinics should stop using the devices immediately and follow recall instructions.
B. Braun Medical recalled 27,480 extension sets used with Infusomat Space Large Volume Pump and related pumps after identifying a backflow and priming risk. The catalog number is 490234 and the primary UDI-DI is 04046964716362. The recall is active worldwide as of 2025-12-03.
B. Braun Medical recalled 10,536 Anesthesia IV Sets sold through multiple retailers worldwide after a potential backflow from piggyback to primary IV lines and occlusion. The devices are used with Infusomat Space Large Volume Pumps, Outlook Pumps, and Vista Basic Pumps. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
B. Braun Medical Inc. recalled 19,320 Anesthesia IV Sets used with Infusomat Space Large Volume Pumps and related BBMI devices sold worldwide through healthcare facilities. The devices pose a backflow risk from secondary piggyback IV containers into the primary IV container and cannot be primed. Healthcare facilities and patients should stop using the device immediately and follow the manufacturer
B. Braun Medical Inc. recalled 9,500 IV administration sets with worldwide distribution including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow medication from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer's recall’s,[
One unit of the Siemens MAMMOMAT Fusion operator table is recalled after being sold with a bus-installation kit. The device is not intended for bus installations and is designed for stationary operation. Health care providers should stop using the device immediately and follow the manufacturer’s recall instructions.
Scepter B62 dual-chamber fuel containers are recalled in Canada after import by Pro Recycle. The units lack flame-mitigation devices and have non-child-resistant closures. Stop using the containers immediately, keep them out of reach of children, and contact Pro Recycle for a full refund.
Olympia Tools International recalls Pack-N-Stroll Premium Folding Utility Wagons sold at Costco after authorities determined the product can trap a child’s head and cause serious injury or death. The defect is an opening between the organizational tray and the sidewall. The wagon also lacks a restraint system. Stop using the wagon now and return it to Costco for a full refund.
Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.