Products may not have received adequate sterilization processing.
Reason for recall: Products may not have received adequate sterilization processing. Distribution: U.S.: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA O.U.S.: Canada Quantity: 93,700 Lot/code info: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 Lot Number: 26025260 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 Lot Number: 26035455 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Lot Number: 26055528
10885403236235, 10885403274619, 10885403237218
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.