Official recall notice

FDA DeviceClass IINotable

FDA Recall: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Ne

Recall date
2026-08-19
FDA class
Class II

Why it was recalled

Hazard

Products may not have received adequate sterilization processing.

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Product description

Products may not have received adequate sterilization processing.

Affected products

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

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