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.
B Braun Medical recalls 12,168 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The backflow of medication from secondary to primary containers and the inability to prime pose a high-risk issue. Stop using the device immediately and follow manufacturer instructions.
B Braun Medical recalls 12,200 IV administration sets sold to hospitals and medical distributors worldwide. The devices labeled NF1503 and catalog number 490062 may allow backflow of medication from secondary piggyback IV containers into primaries and may fail to prime. Hospitals should stop using the devices and follow the 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 recalled 1,250 IV administration sets distributed worldwide to hospitals and clinics. The devices may allow backflow of medication from secondary (piggyback) IV containers into primary containers and may not prime properly. Hospitals and other healthcare providers should stop using the devices immediately and follow recall instructions.
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 its IV Administration Set used with Infusomat Space Large Volume Pumps and related models. The recall cites backflow of medication from secondary to primary IV containers and an occlusion that prevents priming. Hospitals and clinicians should stop using the device immediately and follow manufacturer recall instructions.
B Braun Medical Inc. recalled 41,016 IV administration sets sold worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices pose a risk of backflow from secondary piggyback IV containers into primary containers and may fail to prime. Healthcare providers and patients should stop using the device immediately and follow recall instructions sent by letter.
B. Braun Medical recalls 25,728 IV administration sets sold worldwide, including the United States and Canada. The quad manifold 120-inch IV set may allow backflow from piggyback containers into primary containers and cannot be primed. Healthcare providers should stop using immediately and follow recall instructions.
B. Braun Medical Inc. recalls 40,992 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps sold to hospitals worldwide. The recall targets the IV administration set catalog number 490245. The defect is backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Healthcare providers and patients should stop using theDevice
6,768 IV administration sets are recalled worldwide by B Braun Medical. The recall covers devices used with gravity and pump systems. The hazard is potential backflow of medication into primary IV containers and inability to prime. Stop using the product and follow the recall instructions immediately. Contact B Braun Medical for instructions via the FDA recall page linked below.
B. Braun Medical recalls 286,400 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices may backflow from secondary IV containers into primary containers and cannot be primed. Stop using the device immediately and follow recall instructions from the manufacturer.
B. Braun Medical Inc recalled 5,900 IV administration sets worldwide, including the United States, after reports of backflow from piggyback to primary IV containers and potential priming failure. The devices are used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Hospitals and clinics should stop using the sets and follow manufacturer recall instructions.
B. Braun Medical recalled 29,900 IV administration sets distributed worldwide through medical distributors. The recall is linked to backflow from secondary to primary IV containers and an inability to prime. Healthcare providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.
B Braun Medical recalls 19,104 IV Administration Sets distributed worldwide, including the United States and international distribution to Canada, Germany, Guatemala, and Singapore. The recall cites backflow of medication from secondary piggyback IV containers into primary IV lines and an inability to prime due to occlusion. The affected catalog number is 490400. Stop using the device and follow a
B. Braun Medical recalled 15,250 PB1500 15-DROP IV SETS distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The devices pose a backflow risk from secondary IV containers into primary containers and may fail to prime. Healthcare facilities should stop using the product and follow recall instructions.
B. Braun Medical Inc. is recalling 65,232 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices pose a risk of backflow from secondary piggyback IV containers into primary IV containers and may fail to prime due to occlusion. Hospitals and healthcare providers should stop using the affected sets immediately and follow the maker
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 Inc. recalled 18,072 Outlook IV Sets used with the Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices pose a risk of backflow of medication from secondary IV containers into the primary and an occlusion that can prevent priming. Healthcare providers and patients should stop using the device immediately and follow recall instructions sent by mail.
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 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.