Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Starburst Talon Semi-Flex Electrosurgical Device Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to The devices are not labelled correctly. End users...
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. (Navilyst Medical Inc.) directly.
Affected Products
Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
Quantity: 30
Why Was This Recalled?
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
Where Was This Sold?
This product was distributed to 5 states: LA, MA, OR, VA, WA
About Angiodynamics Inc. (Navilyst Medical Inc.)
Angiodynamics Inc. (Navilyst Medical Inc.) has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report