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Angiodynamics Inc. (Navilyst Medical Inc.) recalls Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-
Recalled November 27, 2019 · FDA recall Z-0411-2020 · Angiodynamics Inc. (Navilyst Medical Inc.)
Hazard
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay. · FDA Class II
Units
30
Sold at
The products were distributed to the following US states: LA, MA, OR, VA, and WA.
Description
The devices are not labelled correctly. End users impacted by this issue may experience a procedural delay.
Product
Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151
Manufacturer(s)
Angiodynamics Inc. (Navilyst Medical Inc.)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →