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: 1,097,048 units Lot/code info: Product Code: 1183500777; UDI/DI: 10192253034691 - each, 20192253034698 - box, 50192253034699 - case; Lot Numbers: 221201, 230201, 230601, 230602
10192253034691, 20192253034698, 50192253034699
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.