BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010

Recalling company

BD SWITZERLAND SARL

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.

Reason

Products may not have received adequate sterilization processing.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Jun 16, 2026

Reported

Aug 19, 2026

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

Status

Ongoing

Quantity

93,700

Lot / codes

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

Company location

Eysins

Recall type

Voluntary: Firm initiated

Recall number

Z-2941-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2941-2026 in the FDA Enforcement Report. Also see FDA recall press releases.