Demonstrated recognition and compatibility issues with syringe infusion pumps.
Reason for recall: Demonstrated recognition and compatibility issues with syringe infusion pumps. Distribution: US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY. Quantity: 3,113,846 units Lot/code info: Product Code: 1180100777; UDI/DI: 10192253034530 - each, 20192253034537 - box, 50192253034538 - case; Lot Numbers: 221201, 221202, 221203, 230201, 230202, 230203, 230204, 230205, 230601
10192253034530, 20192253034537, 50192253034538
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.