inforMED
InjuryLMD

AIDA

Received Aug 12, 2024 · Event occurred Aug 1, 2024

Report 2020550-2024-00290 · MDR key 19961844

Device

Generic name

Aida

Model number

WD200

Catalog number

WD200

Product problems

  • Unintended Application Program Shut Down
  • Unintended Application Program Shut Down

Patient

NA · Unknown

  • Insufficient Information
  • Insufficient Information

Narrative

Description of Event or Problem

IT WAS REPORTED THAT THE DEVICE FAILED DURING THE SURGERY AND A CRACKING NOISE COULD BE HEARD. THE SURGERY HAD TO BE CANCELED.

Additional Manufacturer Narrative

THE AFFECTED DEVICE HAS BEEN REQUESTED FOR INVESTIGATION BY THE MANUFACTURER. THE INVESTIGATION IS NOT COMPLETED YET. THE INVESTIGATION RESULTS ARE PENDING. THE EVENT IS FILED UNDER INTERNAL KARL STORZ COMPLAINT ID: (B)(4).