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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:162989

Atelia IM 1300 Analyzer for in vitro diagnostic testing of clinical specimens.

Official recall number

Z-1586-2018

Evidence summary

Product code
JJE
Recall status
Terminated
Event initiated
February 26, 2018
Root cause
Software design
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-1586-2018

Field note

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