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: 3,084,300 units Lot/code info: Product Code: 1181200777T; UDI/DI: 10192253025811 - each, 20192253025818 - box, 50192253025819 - case; Lot Numbers: 221101, 221102, 221103, 221104
10192253025811, 20192253025818, 50192253025819
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.