medical Class II Updated 2020-11-11

Angiodynamics, Inc. recalls Angiodynamics 5F Standard Micro-Introducer Kit - indicated f

Recalled 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

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Number: 5626935 Expiration Date: 08/31/2023
View official government recall

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