FDAClass II · Medical device · Recall Z-2941-2026 · Recalled August 19, 2026

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall — BD SWITZERLAND SARL

Agency report date: August 19, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code
Company / brand: BD SWITZERLAND SARL
Lot / serial / date 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
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

Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Products may not have received adequate sterilization processing.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2941-2026
Brand: All BD SWITZERLAND SARL recalls
Classification: Class II
Units affected: 93,700
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall status

Companies & origin

Recalling firm location: Eysins, Switzerland
Firm address: Terre Bonne Park A4, Route De Crassier 17, N/A

Identifying details (verbatim from the notice)

Product codes / lots: 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
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
Firm notified the public via: Letter
FDA event ID: 99264
Recall initiated: June 16, 2026
FDA classified: August 13, 2026
FDA report date: August 19, 2026

More BD SWITZERLAND SARL recalls

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusi recall — BD SWITZERLAND SARLFDA · September 23, 2026

Other medical device recalls from around the same time

Boston Scientific ENROUTE Transcarotid Neuroprotection System recall — Boston Scientific CorporationFDA · August 26, 2026
BD Needle Kit for Powered Driver 15mm x 15Ga recall — Bard Access Systems, Inc.FDA · August 26, 2026
Brand Name recall — Spectra Medical Devices, LlcFDA · August 19, 2026
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall — Baxter Healthcare CorporationFDA · August 19, 2026
INFINION CX LEAD KIT recall — Boston Scientific Neuromodulation CorporationFDA · August 12, 2026

Verify with the official sources:

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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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