InjuryMBV
ZIMMER SEGMENTAL DISTAL FEMORAL COMPONENT
Received Apr 4, 2013
Report 1822565-2013-00605 · MDR key 3042099
Device
Generic name
Knee Prosthesis
Manufacturer
Zimmer, Inc.Product problems
- Migration or Expulsion of Device
Patient
Not reported
- No Information
Narrative
Description of Event or Problem
IT IS REPORTED THAT THE PATIENT WAS REVISED DUE TO THE SCREW BACKING OUT. IT IS ALSO REPORTED THAT THE SCREW WAS ORIGINALLY IMPLANTED ON THE WRONG SIDE OF THE FEMORAL COMPONENT.
Additional Manufacturer Narrative
THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.