Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F Recalled by Angiodynamics Worldwide Headquarters Due to Mislabeling
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 Worldwide Headquarters directly.
Affected Products
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA. Intended use: angiographic diagnosis.
Quantity: 7 boxes/35 units
Why Was This Recalled?
AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because one of the catheter pouches within the outer box may be mislabeled.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Angiodynamics Worldwide Headquarters
Angiodynamics Worldwide Headquarters has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report