1,814 product recalls found in this category. Browse through all safety alerts and stay informed.
High Activity Category
This category has a significant number of recalls. Please check regularly for updates.
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 4,536 IV administration sets globally after reports of backflow risk and occlusion. The sets labeled catalog 490437 are used with gravity IV administration and pump systems such as Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Patients and healthcare providers should stop using the devices immediately and follow the recall instructions.
B. Braun Medical recalled 1,861,111 IV Administration Sets sold globally through hospitals and medical distributors. The sets may allow backflow from secondary to primary IV containers and cannot be primed. Hospitals and clinicians using these sets with Infusomat Space, Outlook, or Vista Basic Pumps should stop using them immediately and contact B. Braun Medical for instructions.
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 381,850 CareSite IV sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump after concerns about backflow and occlusion. The defect could allow medication to flow from secondary piggyback IV containers into primary IV containers and prevent priming. Hospitals and clinicians should stop using the affected devices immediately and follow recall,厂
B. Braun Medical recalled the Outlook IV Set 15DR W/2 CARESITE FILTER (Catalog 354214) used with Infusomat Space pumps and BBMI devices. The recall cites backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions by mail.
B Braun Medical Inc. recalled 100 units of the V1782F Univ IV Set W/0.2 MICRON FILTER, distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore. The sets may allow backflow from secondary piggyback IV containers into primary IV containers and cannot be primed. Healthcare facilities should stop using the devices immediately and follow the 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.
BBraun Medical recalled 5,448 Blood Administration Sets used with Infusomat Space pumps worldwide sold to hospitals. The recall cites potential backflow of medication from secondary piggyback IV containers into primary IV containers and an inability to prime. Healthcare facilities should stop using the sets immediately and follow recall instructions from B. Braun Medical.
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 18,984 IV administration sets after discovering a potential for backflow of medication from secondary IV containers into primary containers. This defect creates a high risk of medication errors and occlusion. Patients and healthcare providers should stop using these sets immediately and contact B Braun Medical for further instructions.
B. Braun Medical recalled 3,120 IV administration sets distributed worldwide to hospitals and clinics. The recall concerns potential backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by the manufacturer.
B. Braun Medical recalled 66,792 IV Administration Sets sold worldwide through multiple healthcare distributors after reports of backflow and priming occlusion risk. The devices labeled catalog numbers 490241, 490298, and 490360 may allow medication to backflow from piggyback containers into primary lines and may fail to prime. Hospitals and clinicians should stop using immediately and follow the厂
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 Inc. recalls 36,936 IV administration sets used with Infusomat Space and other pumps worldwide. The recall was announced Oct. 29, 2025 and includes US and international distribution to Canada, Germany, Guatemala and Singapore. The devices may allow backflow of medication from secondary containers into the primary container and cannot be primed. Stop using immediately and follow the
B. Braun Medical has issued an active recall for 45,288 IV administration sets catalog 490412. The devices support gravity and pump-based IV administration with Infusomat Space, Outlook, and Vista Basic Pumps. The recall cites a design defect that can allow backflow from secondary piggyback containers into primary IV lines and prevent priming.
B Braun Medical recalled 98,568 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall covers catalog number 490274 and UDI-DI codes. The device presents a backflow risk and inability to prime. Hospitals and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
B. Braun Medical Inc. recalled 5,952 IV Administration Sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore, for use with Infusomat Space, Outlook, and Vista Basic Pumps. The units carry Catalog Number 490612. The recall cites potential backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare teams
B. Braun Medical recalled 259,392 IV administration sets worldwide on Oct. 29, 2025. The devices could allow backflow of medication from secondary (piggyback) IV containers into primary IV containers and may not prime due to occlusion. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions in the notice.