Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Starburst MRI Semi-Flex Electrode Device Recalled by Angiodynamics Due to Printed mark on the trocar intended to indicate...
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 directly.
Affected Products
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615
Quantity: 43
Why Was This Recalled?
Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually located 4cm from the distal tip of the needle.
Where Was This Sold?
This product was distributed to 11 states: AZ, AR, FL, MI, MN, MO, NY, TX, VA, WA, WI
About Angiodynamics
Angiodynamics 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