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FDA (Device enforcement)Recalled 2026-06-16class ii

BD SWITZERLAND SARL: 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

Hazard

Products may not have received adequate sterilization processing.

Details from the source

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

UPC codes

10885403236235, 10885403274619, 10885403237218

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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