InjuryFCX
ENDOFLATOR 40
Received Jun 23, 2026
Report 9610617-2026-01442 · MDR key 25600256
Device
Product problems
- Output Problem
Patient
NA · Unknown
- Insufficient Information
Narrative
Additional Manufacturer Narrative
THE AFFECTED DEVICE HAS BEEN REQUESTED FOR INVESTIGATION BY THE MANUFACTURER. THE DEVICE WAS NOT YET RETURNED FOR INVESTIGATION. THE EVENT IS FILED UNDER INTERNAL KARL STORZ COMPLAINT ID: (B)(4).
Description of Event or Problem
THE FOLLOWING WAS REPORTED: "ENDOFLATOR UNEXPECTEDLY STOPPED WORKING. SURGEON WAS COMPELLED TO COMPLETE THE PROCEDURE THROUGH OPEN SURGERY."