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FDAOctober 14, 2020device

Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355

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

The hazard

5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component

What to do

FDA enforcement status: Terminated

Brands named

angiodynamics

Recall history

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

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Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355 — Recall Details · AllClear