FDA Adverse Event Other Summary report: N

HIP

MDR report key: 540743 · Received March 25, 2004

Report

Report Number
1043534-2004-00018
Event Type
Other
Date Received
March 25, 2004
Report Date
February 24, 2004
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
JDI
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

ORIG. SURG. 1999. ALLEGEDLY HIP IMPLANT FAILED PER CONTACT. NO OTHER INFO IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HIP HIP COMPONENT JDI WRIGHT MEDICAL TECHNOLOGY, INC. NI NI

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Other