425 recalls tagged with “burn risk”.
B Braun Medical recalled 46,250 IV administration sets on October 29, 2025. The recall follows concerns about potential backflow of medication into primary IV containers. The affected products were sold worldwide, including the US and Canada.
B Braun Medical recalled 3,120 IV administration sets on October 29, 2025, due to a risk of medication backflow. The recall affects models used with Infusomat Space, Outlook, and Vista Basic Pumps. The company advises patients and healthcare providers to stop using the devices immediately.
B Braun Medical recalled 66,792 IV Administration Sets on October 29, 2025, due to a potential backflow risk. The recall affects models used with Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers must stop using these devices immediately.
B Braun Medical recalled 122,232 IV administration sets on October 29, 2025. The recall addresses potential backflow of medication from secondary IV containers into primary containers. Affected units were distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore.
B Braun Medical recalled 2,544 IV Administration Sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled 63,192 IV Administration Sets on October 29, 2025. The recall affects sets used with the Infusomat Space, Outlook, and Vista Basic Pumps. The company reported a risk of medication backflow and occlusion.
B Braun Medical recalled 5,100 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. The product poses a high risk of medication backflow from secondary IV containers.
B Braun Medical recalled 36,936 IV Administration Sets on October 29, 2025. The recall stems from a potential backflow of medication from secondary IV containers into primary IV containers. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled 45,288 IV administration sets on October 29, 2025. The recall addresses a risk of backflow from secondary IV containers into primary containers. Users must stop using the product immediately and follow manufacturer instructions.
B Braun Medical recalled 98,568 IV administration sets on October 29, 2025. The recall affects sets labeled as Catalog Number 490274 due to a risk of medication backflow. Healthcare providers and patients should stop using these devices immediately.
B Braun Medical recalled 5,952 IV administration sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers. This poses a serious health risk for patients receiving treatment.
B Braun Medical recalled 12,200 IV Administration Sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista pumps. The recall addresses the risk of medication backflow and occlusion issues.
B Braun Medical recalled 190,625 IV administration sets on October 29, 2025. The recall addresses a potential backflow of medication from secondary IV containers. Healthcare providers must stop using the device immediately to prevent serious complications.
B Braun Medical recalled 41,976 IV administration sets on October 29, 2025. The recall stems from a risk of medication backflow into primary IV containers. Affected products include catalog number 490354, distributed worldwide.
B Braun Medical issued a recall for 1,250 IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication between IV containers, posing a serious risk to patients. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 7,008 IV administration sets on October 29, 2025. The recall stems from the potential backflow of medication from secondary IV containers. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled IV Administration Sets on October 29, 2025, due to a backflow risk. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers should stop using the product immediately.
B Braun Medical recalled 25,728 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 40,992 IV administration sets on October 29, 2025. The recall addresses a potential for backflow of medication from secondary IV containers into primary containers. This issue may lead to serious health risks for patients.
B Braun Medical recalled over 20 million IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication that could put patients at risk. Healthcare providers and patients must stop using the devices immediately.