Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015) Recalled by Angiodynamics, Inc. Due to Product was placed into distribution prior to completion...
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
Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201 AngioDynamics Angiographic Catheters are for use where angiographic diagnosis is indicated.
Quantity: 28
Why Was This Recalled?
Product was placed into distribution prior to completion of all required post sterilization release activities.
Where Was This Sold?
This product was distributed to 14 states: AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX
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