5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Check against the official notice below — it lists the full affected range.
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovolemia.
Reason for recall: Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovolemia. Distribution: Worldwide - US Nationwide distribution in the states of AL, CA, CO, FL, GA, IL, KY, LA, MA, MD, MN, MO, NC, NH, NH, NY, OH, PA, TN, TX, VA and the country of Lithuania. Quantity: 6,624 units Lot/code info: Lots 25JR01802 25NR01017 25NR01266 UDI-DI 00840861102525
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.