InjuryFCX
ENDOFLATOR 40
Received Jul 27, 2026 · Event occurred May 25, 2026
Report 9610617-2026-01728 · MDR key 50017293
Device
Product problems
- Output Problem
Patient
Not reported
- Insufficient Information
Narrative
Description of Event or Problem
The following was reported: For the patient with appendicitis, a device system failure alert popped out after anesthesia before surgery, forcing the operation to be aborted. After physician consultation, traditional open resection was performed. The patient has been discharged normally.
Additional Manufacturer Narrative
Under user's discretion the device in question will not be returned to manufacturer for evaluation. The investigation will be performed by a designated KARL STORZ employee, investigation results are pending.The event is filed under internal KARL STORZ complaint ID: (b)(4).