Home / Recalls / Medical Devices
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site
Recalled August 19, 2026 · FDA recall Z-2941-2026 · BD SWITZERLAND SARL
Hazard
Products may not have received adequate sterilization processing. · FDA Class II
Units
93,700
Sold at
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
Description
Products may not have received adequate sterilization processing.
Product
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Intravascular Administration Set and Extension Set used to administer fluids.
Manufacturer(s)
BD SWITZERLAND SARL
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →