FDA Adverse Event Injury Summary report: N

DEPUY

MDR report key: 1071108 · Received July 7, 2008

Report

Report Number
1071108
Event Type
Injury
Date Received
July 7, 2008
Date of Event
May 15, 2008
Report Date
June 19, 2008
Manufacturer
DEPUY MANUFACTOR
Product Code
JDI
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BROKEN HIP PROSTHESIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DEPUY DEPUY METAL HIP PROSTHESIS JDI DEPUY MANUFACTOR

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization