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Recall Observatory FDA recall evidence

Derived label

Device software or design

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for general diagnostic use

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
incorrect software
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
GE Healthcare, LLC

Field note

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