Reported Aug 19, 2026 · Ongoing · Updated Sep 16, 2026
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site…
Bd Switzerland Sarl
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: BD SWITZERLAND SARL · Terre Bonne Park A4, Route De Crassier 17 · Eysins
Is this the product you have?
- 60 In Non-DEHP Minibore
- Extension Set RES ME2010 UDI-DI code10885403236235 MaxPlus Ext Set w/Needleless
- and Y-Site REF MPX5305-C UDI-DI code10885403274619 9 IN Extension
- Set w/Max Y REF MPX5300-C UDI-DI code10885403237218 Intravascular Administration Set and Extension Set used to administer fluids
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published — Lot Number: 26025260 MaxPlus Ext Set w/Needleless and Y-Site MPX5305-C10885403274619UDI-DI code: 10885403274619 — Lot Number: 26035455 9 IN Extension Set w/Max Y MPX5300-C10885403237218UDI-DI code: 10885403237218 — Lot Number: 26055528 - Amount recalled
- 93,700
Where it was sold
Why it was recalled
Products may not have received adequate sterilization processing.
This product could cause temporary or reversible health problems — stop using it.
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