60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code:… — Class II medical device recall Z-2941-2026
Ongoing recall by BD SWITZERLAND SARL, reported 2026-08-19, distributed in AZ, CA, CO, FL, GA, IL, IN, KS…. Products may not have received adequate sterilization processing.
| Recall number | Z-2941-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | BD SWITZERLAND SARL, Eysins, Switzerland |
| Recall initiated | 2026-06-16 |
| Classified | 2026-08-13 |
| Reported by FDA | 2026-08-19 |
| Distributed | 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 |
| Countries outside the US | CA |
| Quantity | 93,700 |
| UPC / GTIN / UDI-DI | 10885403236235, 10885403237218, 10885403274619 |
| Lot numbers | 26025260, 26035455, 26055528 |
| Model numbers | MPX5300-C, MPX5305-C |
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 for recall
Products may not have received adequate sterilization processing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2941-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.