FDA Adverse Event Injury Summary report: N

ZIMMER GENDER SOLUTIONS ARTICULAR SURFACE

MDR report key: 2003833 · Received February 24, 2011

Report

Report Number
1822565-2011-00400
Event Type
Injury
Date Received
February 24, 2011
Date of Event
June 18, 2010
Report Date
January 27, 2011
Manufacturer
ZIMMER, INC.
Product Code
MBH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

Description of Event or Problem · 1

IT IS REPORTED THAT THE PATIENT UNDERWENT SURGERY TO DRAIN A HEMATOMA AND REPAIR A RETINACULAR TEAR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ZIMMER GENDER SOLUTIONS ARTICULAR SURFACE MBH ZIMMER, INC. 60839751

Patients

Seq Age Sex Outcome Treatment
1 68 YR Required Intervention