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: 4,913,520 units Lot/code info: Product Code: 1182000777; UDI/DI: 10192253034677 - each, 20192253034674 - box, 50192253034675 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206
10192253034677, 20192253034674, 50192253034675
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.