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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:177122

Starburst Talon Semi-Flex Electrosurgical Device, Part Number H7877001028451 incorrectly labelled as Starburst MRI Semi-Flex Electrosurgical Device, Part Number H7877001026151

Official recall number

Z-0411-2020

Evidence summary

Product code
GEI
Recall status
Terminated
Event initiated
October 02, 2019
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0411-2020

Field note

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