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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:156955

IMPAX Cardiovascular The IMPAX CV Reporting module consists of a database and graphical user interface (GUI) that allows users to document procedure and clinical findings as structured data, with representation in printed or electronic formats

Official recall number

Z-2652-2017

Evidence summary

Product code
LLZ
Recall status
Terminated
Event initiated
December 22, 2016
Root cause
Software design
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2652-2017

Field note

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