FDA Adverse Event Injury Summary report: N

INFINITY COLLARED TROCHANTERIC PRESS-FIT MODULE

MDR report key: 116669 · Received August 29, 1997

Report

Report Number
1043534-1997-00135
Event Type
Injury
Date Received
August 29, 1997
Date of Event
April 23, 1997
Report Date
May 27, 1997
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
JDI
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION STATEMENT: THERE WAS NO DEVICE FAILURE. DEVICE WAS MANUFACTURED AND SOL BY DOW CORNING WRIGHT, WHO ASSETS WERE PURCHASED BY WRIGHT MEDICAL TECHNOLOGY, INC.

Description of Event or Problem · 1

REVISION SURGERY WAS PERFORMED FOR AN ALLEGEDLY BROKEN STEM. THIS COMPONENT WAS REVISED AT THAT TIME. NO COMPLAINT WAS STATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INFINITY COLLARED TROCHANTERIC PRESS-FIT MODULE Implant HIP COMPONENT - DEVICE 2 JDI WRIGHT MEDICAL TECHNOLOGY, INC. NA M692850

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Required Intervention