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Recall Observatory FDA recall evidence

Derived label

Device software or design

Monarch Platform REF MON-000005-01R, 100-240V- 50/60Hz 1440w

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software issues may result in
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
AURIS HEALTH INC

Field note

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