Home / Recalls / Medical Devices
Access Vascular, Inc recalls HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous acces
Recalled March 1, 2023 · FDA recall Z-1156-2023 · Access Vascular
Hazard
Label with the incorrect component listed on the inner kit Tyvek header bag · FDA Class II
Units
445 units
Sold at
US Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.
Description
Label with the incorrect component listed on the 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 Number: 80004004
Manufacturer(s)
Access Vascular, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →