Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction Recalled by Angiodynamics, Inc. Due to 5F Micro-Introducer Kits may not contain the correct...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Angiodynamics, Inc. directly.
Affected Products
Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355
Quantity: 32 kits
Why Was This Recalled?
5F Micro-Introducer Kits may not contain the correct device, packaged with a 4F Sheath/Dilator component
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Angiodynamics, Inc.
Angiodynamics, Inc. has 74 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report