Class II — BD SWITZERLAND SARL
| Recalling firm | BD SWITZERLAND SARL |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| Quantity | 93,700 |
| 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 |
| Initiated | 2026-06-16 |
| Classified | 2026-08-13 |
| Recall number | Z-2941-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — BD SWITZERLAND SARL (Z-2941-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99264/
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