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Angiodynamics, Inc. recalls Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter int
Recalled November 11, 2020 · FDA recall Z-0418-2021 · Angiodynamics
Hazard
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component · FDA Class II
Units
32 kits
Sold at
US Nationwide distribution including in the states of AL, CT, GA, FL.
Description
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component
Product
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355
Manufacturer(s)
Angiodynamics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →