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FDADecember 22, 2022device

HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Model Number: 80004004

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Product Mislabeled on the outer bag and inner kit Tyvek header bag

What to do

FDA enforcement status: Ongoing

Brands named

access vascularaccess

UPCs

00850030354020

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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