794 recalls tagged with “infant product”.
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 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.
BBraun Medical recalled 12,700 ADDitIV gravity IV sets distributed worldwide. The sets can backflow medication from piggyback containers into primary IV containers and cannot be primed. Healthcare providers and patients should stop using the sets immediately and follow the recall instructions from BBraun Medical.
B. Braun Medical Inc. recalled 12,225,913 CARESITE gravity IV sets and pump sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may backflow medication from secondary to primary IV containers and fail to prime. Healthcare facilities and patients should stop using immediately and follow the recall instructions from the manufacturer. For refund or replacement inquiries,联系
B. Braun Medical recalled 65,904 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The recall cites backflow of medication from secondary (piggyback) IV containers into primary containers and an inability to prime. Hospitals should stop using the devices immediately and follow the manufacturer's recall instructions.
B. Braun Medical Inc. recalls 31,392 IV administration sets used with Infusomat Space and other pumps worldwide. The device may allow backflow from piggyback containers into primary IV lines and cannot be primed. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions.
BBraun Medical Inc recalls 960 IV administration sets distributed worldwide due to backflow risk and inability to prime. The recall affects the IV administration set catalog number 490491 with UDI-DI 04046955086931. The device can allow medication to flow from secondary piggyback containers into primary IV containers and may not prime properly. Stop using immediately and follow recall instructions
BBMI Medical recalled 20,694,734 IV administration sets due to backflow risk and occlusion in piggyback configurations. The recall covers sets used with Infusomat Space, Outlook, and Vista Basic Pumps. Stop using the devices immediately and follow manufacturer instructions.
B Braun Medical Inc. recalls 5,100 IV administration sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The recall cites backflow of medication from piggyback containers into primary IV containers and an occlusion that prevents priming. Patients should stop use immediately and follow recall instructions.
B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow
B Braun Medical Inc. recalls 43,900 ADDitIV gravity and pump administration sets. The recall covers catalog numbers V1443, V1447, V1448, and V1484. The issue is backflow of medication from secondary IV containers into primary containers and inability to prime the line. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.
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.
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 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
Twin Sisters Creamery recalled 411 pounds of Whatcom Farmhouse cheese sold through Whole Foods Market after testing flagged potential STEC and E. coli O103 contamination. The recall is Class I. Consumers who bought this product should not eat it and should contact WFM Purchasing, LP for refund or replacement information.
Siemens Medical Solutions USA recalls the MAMMOMAT Inspiration operator table. The recall covers six units worldwide, including three in the United States. The operator table was sold with a bus-installation kit and is not designed or released for bus installations. Stop using the device immediately and contact Siemens for instructions.
Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek 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.
Canada Prep and Ship recalled Scepter B62 dual-chamber gas and oil fuel containers imported for safety reasons. The recall cites fire and burn hazards from lacking flame-mitigation devices and non–child-resistant closures. Stop using the containers and contact Canada Prep for a full refund.
No injuries have been reported. Cranach Hardware recalled tip restraint kits sold through retailers after testing showed the plastic brackets and tie can fail to meet safety standards. Stop using the restraints and contact Cranach Hardware for a free stainless steel replacement kit.