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: 3,936,682 units Lot/code info: Product Code: 1180600777; UDI/DI: 10192253034608 - each, 20192253034605 - box, 50192253034606 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206, 230207
10192253034608, 20192253034605, 50192253034606
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.