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.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
B Braun Medical recalled 18,072 IV administration sets on October 29, 2025. The recall affects the Outlook set utilized with Infusomat Space and Outlook Pumps. The sets pose a high risk of medication backflow and priming issues.
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 150,664 IV administration sets on October 29, 2025. The recall affects products identified by catalog number 375258. These devices pose a high risk of medication backflow from secondary IV containers.
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 100 IV administration sets on October 29, 2025, due to a backflow risk. The recall affects gravity IV and pump administration sets used with several infusion pumps. The potential for medication backflow poses a serious health risk to patients.
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 187,464 IV administration sets on October 29, 2025. The recall stems from the potential for medication backflow and occlusion. The affected products were distributed worldwide, including the U.S. and Canada.
B Braun Medical recalled 11,832 IV administration sets on October 29, 2025. The recall affects models catalog numbers 490315, 490331, and 490376. The device poses a risk of medication backflow and occlusion during use.
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 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 approximately 259,392 IV Administration Sets on October 29, 2025, due to a risk of medication backflow. The recall affects products with catalog number 490309 distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore.
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 12,320 burette sets on October 29, 2025, due to a risk of medication backflow. This defect can lead to serious health risks for patients. The recall affects devices distributed worldwide, including the U.S., Canada, Germany, Guatemala, and Singapore.