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Recall Observatory FDA recall evidence

Derived label

Device software or design

Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software version 02-xx, only when rack buffering is activated and the rack buffer is completely full. This issue can
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Roche Diagnostics Corporation

Field note

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