1,030 recalls tagged with “electrical hazard”.
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 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 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 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 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 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 7,344 blood administration sets on October 29, 2025. The recall follows a potential backflow hazard that could affect patient safety. Healthcare providers must stop using the affected devices immediately.
B Braun Medical recalled 5,448 blood administration sets on October 29, 2025. The recall affects devices used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The company cited potential backflow of medication and occlusion as the primary hazards.
B Braun Medical recalled 43,900 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Users must stop using these devices immediately due to a potential medication backflow hazard.
B Braun Medical recalled 12,700 IV administration sets on October 29, 2025, due to a risk of medication backflow. The affected models include Catalog Number 352062, distributed worldwide including the US, Canada, and Germany. Healthcare providers must stop using these devices 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 554,015 IV administration sets on October 29, 2025. The recall addresses a high risk of medication backflow into primary IV containers. Patients and healthcare providers must stop using these sets immediately.
B Braun Medical recalled over 49 million IV administration sets on October 29, 2025. The recall addresses a potential backflow of medication from secondary IV containers into primary IV containers. Users should stop using the affected devices immediately.
B Braun Medical recalled 33,528 blood administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista Basic Pumps. The devices pose a backflow risk that could compromise patient safety.
B Braun Medical recalled 162,648 IV administration sets on October 29, 2025. The products pose a high risk of backflow from secondary IV containers into primary containers. Affected sets include catalog number 354212, distributed worldwide.
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 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.
Medtronic recalled 6,591 extravascular implantable cardioverter defibrillators on October 29, 2025. The recall stems from a potential delay in high-voltage therapy that could occur under rare conditions. Patients must stop using the devices immediately and follow manufacturer instructions.
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.
Philips North America recalled 2,341 Incisive CT scanners on October 29, 2025. A component may detach and damage other parts during operation. Users must stop using the device immediately and follow recall instructions.