InjuryNDF
ZIMMER PERIARTICULAR HUMERAL PLATE
Received Mar 22, 2013
Report 1822565-2013-00520 · MDR key 3022656
Device
Manufacturer
Zimmer, Inc.Catalog number
00234800606
Product problems
- Fracture
- Insufficient Device Problem Information
Patient
Not reported
- Foreign Body Reaction
Narrative
Description of Event or Problem
IT IS REPORTED THAT THE PATIENT IS EXPERIENCING A POSSIBLE ALLERGIC REACTION. X-RAYS NOTED A BROKEN SCREW.
Additional Manufacturer Narrative
THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.