MalfunctionGFD
ZIMMER AIR DERMATOME
Received Jun 24, 2026
Report 0001526350-2026-00731 · MDR key 25616108
Device
Product problems
- Unstable
Patient
NA · Unknown
- Insufficient Information
Narrative
Additional Manufacturer Narrative
(B)(4). G2: FOREIGN - EVENT OCCURRED IN CANADA. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED.
Description of Event or Problem
IT WAS REPORTED THAT DURING AN UNKNOWN TIME, THE UNIT WAS SKIPPING. IT IS UNKNOWN IF THERE WAS A PATIENT IMPACT OR IF A DELAY OCCURRED. DUE DILIGENCE IS COMPLETE AND NO ADDITIONAL INFORMATION IS AVAILABLE.