101 recalls found for B. Braun Medical. Check if any of your products are affected.
B. Braun Medical is recalling 21,000 21GA Winged Infusion Sets (Single Pack) distributed worldwide, including Texas and Costa Rica, catalog 7A3842. The needle tip can be dull or blunt, may be difficult to advance, or break. Clinicians and patients should stop using the device and await manufacturer instructions.
B. Braun Medical recalls 51,300 units of its 21GA Winged Infusion Set, model 7M2802, distributed worldwide including Texas and Costa Rica. The device’s needle tip can be dull or break, making advancement difficult. Stop using the device immediately and contact the manufacturer or your healthcare provider for instructions.
B. Braun Medical recalled 105,550 BBraun Medical 21G X4.4CM Winged INF devices worldwide, including Texas and Costa Rica. A dull or blunt needle tip may be difficult to advance or break. Healthcare providers and patients should stop using the device and follow the manufacturer's recall instructions.
B Braun Medical recalled 28,344 IV administration sets on October 29, 2025. The recall affects gravity and pump administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. Users face a high risk of medication backflow into primary IV containers.
B Braun Medical recalled 32,500 IV extension sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled 11,800 IV extension sets on October 29, 2025. The recall follows reports of potential medication backflow from secondary IV containers. Healthcare providers should stop using the device immediately.
B Braun Medical recalled 2,100 IV administration sets on October 29, 2025. The recall follows reports of backflow of medication from secondary IV containers into primary IV containers. This poses a high risk for patients using the Infusomat Space, Outlook, and Vista pumps.
B Braun Medical recalled 300 IV administration sets on October 29, 2025, due to a risk of medication backflow. The defect affects the ability to prime IV containers. Healthcare providers should stop using these devices immediately.
B Braun Medical recalled 1,200 IV extension sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers into primary containers. The affected model is catalog number 490358.
B Braun Medical recalled 61,423 IV administration sets on October 29, 2025, due to a high risk of medication backflow. The recall affects models with catalog numbers 456521 and 456522, distributed worldwide. Patients and healthcare providers must stop using these devices immediately.
B Braun Medical recalled 13,600 IV administration sets on October 29, 2025. The recall affects models catalog number 490202 due to a potential backflow hazard. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled 11,650 IV extension sets on October 29, 2025, due to potential backflow of medication. This defect affects the Infusomat Space, Outlook, and Vista Basic Pumps. Patients must stop using the device immediately and follow recall instructions.
B Braun Medical recalled 10,536 Anesthesia IV Sets on October 29, 2025. The recall stems from a risk of medication backflow between IV containers. Healthcare providers must stop using the product immediately to prevent potential harm.
B Braun Medical recalled 104,784 Anesthesia IV Sets on October 29, 2025. The recall affects models utilized with Infusomat Space, Outlook, and Vista pumps due to potential medication backflow. This hazard poses serious risks for patients receiving IV medication.
B Braun Medical recalled 19,392 anesthesia IV sets on October 29, 2025 due to the potential for medication backflow. The defective sets may cause occlusion and were sold worldwide, including in the US, Canada, Germany, Guatemala, and Singapore.
B Braun Medical recalled 32,436 Anesthesia IV Sets on October 29, 2025. The recall affects specific catalog numbers due to a risk of medication backflow. Healthcare providers must stop using these devices immediately and follow the provided recall instructions.
B Braun Medical recalled 58,752 Anesthesia IV Sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. This poses a high hazard level for patients using the Infusomat Space and other pumps.
B Braun Medical recalled 19,320 Anesthesia IV Sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 23,160 IV administration sets on October 29, 2025. The sets pose a high risk of medication backflow from secondary containers into primary containers. Healthcare providers should stop using the devices immediately.
B Braun Medical recalled 27,480 IV extension sets on October 29, 2025. The recall affects devices tied to the Infusomat Space, Outlook, and Vista pumps. The company warns of potential medication backflow and occlusion issues that could endanger patients.