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Recall Observatory FDA recall evidence

Derived label

Device software or design

ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
software coding error
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Alcon Research, Ltd.

Field note

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