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Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous acce
Recalled March 1, 2023 · FDA recall Z-1155-2023 · Access Vascular
Hazard
Product Mislabeled on the outer bag and inner kit Tyvek header bag · FDA Class II
Units
155 units
Sold at
US Nationwide distribution in the states of FL, TX, WA.
Description
Product Mislabeled on the outer bag and inner kit Tyvek header bag
Product
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
Manufacturer(s)
Access Vascular, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →