Health & Personal Care
HIGH
FDA DEVICE
BBMI IV Administration Sets Recalled in 2025 for Backflow and Occlusion Risk, 20.7 Million Units
BBMI Medical recalled 20,694,734 IV administration sets due to backflow risk and occlusion in piggyback configurations. The recall covers sets used with Infusomat Space, Outlook, and Vista Basic Pumps. Stop using the devices immediately and follow manufacturer instructions.
BBMI Medical
Potential for