FDA Adverse Event Injury Summary report: N

DEPUY

MDR report key: 1021500 · Received March 19, 2008

Report

Report Number
1021500
Event Type
Injury
Date Received
March 19, 2008
Date of Event
July 10, 2007
Report Date
February 8, 2008
Manufacturer
DEPUY A JOHNSON & JOHNSON CO.
Product Code
JDI
Product Problem
Yes
Report Source
User Facility report
Reporter Location
PA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

REMOVAL OF IMPLANTED LEFT HIP PROSTHESIS AND REPLACEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DEPUY HIP PROSTHESIS JDI DEPUY A JOHNSON & JOHNSON CO. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 59 YR Required Intervention