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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:117178

Cobas¿ 8000 modular analyzer series software version 03-01, 02, 03 and 04, impacting the cobas e 602 module only. Product Usage: Fully automated immunoassay analyzer intended for the in-vitro quantitative/qualitative determination of analytes in body fluids. This analyzer is optimized for high throughput workloads in the professional environment using a combination of ion selective electrodes and photometric analysis modules

Official recall number

Z-1368-2013

Evidence summary

Product code
JJE
Recall status
Terminated
Event initiated
April 04, 2013
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1368-2013

Field note

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