These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,324 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
B Braun Medical recalled 24,624 blood administration sets on October 29, 2025, due to a risk of backflow from secondary IV containers. These sets are incompatible with the Infusomat Space, Outlook, and Vista Basic pumps. Healthcare providers must stop using these devices immediately to prevent potential medication errors.
B Braun Medical recalled 960 IV administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista pumps. Users face a high risk of medication backflow and occlusion.
B Braun Medical recalled 111,312 IV administration sets due to a risk of backflow of medication. The sets are used with Infusomat Space, Outlook, and Vista Basic Pump models. The recall was announced on October 29, 2025, following potential safety issues.
B Braun Medical recalled 286,400 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Users must stop using the devices immediately and follow the manufacturer's instructions.
B Braun Medical recalled 1,019 IV administration sets on October 29, 2025. The recall addresses a risk of medication backflow from secondary IV containers. Affected devices include catalog number 457506 and others.
B Braun Medical recalled 4,536 IV administration sets on October 29, 2025. The recall affects devices that may allow backflow of medication from secondary IV containers. This poses a high risk to patients using the Infusomat Space, Outlook, and Vista Basic pumps.
B Braun Medical recalled 6,768 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. The recall addresses a potential backflow issue that could compromise patient safety.
B Braun Medical recalled 74,652 IV administration sets on October 29, 2025. The recall impacts users of the Infusomat Space, Outlook, and Vista Basic Pumps due to backflow risks. The affected catalog number is US9923F, with worldwide distribution including the US and Canada.
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.
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 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 10,896 IV administration sets on October 29, 2025. The recall addresses a risk of medication backflow from secondary IV containers. This issue could lead to serious health risks for patients.
B Braun Medical recalled 1,861,111 IV administration sets on October 29, 2025. The recall addresses a significant risk of medication backflow from secondary IV containers into primary containers. Healthcare providers and patients must 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 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 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 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 381,850 IV administration sets on October 29, 2025. The recall addresses potential backflow of medication from secondary IV containers into primary containers. This issue poses a significant risk to patients and healthcare providers worldwide.
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 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.