FDA Adverse Event Injury Summary report: N

HUNTER TENDON ROD

MDR report key: 1338242 · Received March 5, 2009

Report

Report Number
MW5010237
Event Type
Injury
Date Received
March 5, 2009
Date of Event
September 4, 2008
Report Date
March 5, 2009
Manufacturer
WRIGHT MEDICAL TECHNOLOGY
Product Code
HXA
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IL, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

MD REMOVED HUNTER TENDON ROD- STATED FAILURE OF DEVICE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HUNTER TENDON ROD HUNTER TENDON ROD HXA WRIGHT MEDICAL TECHNOLOGY

Patients

Seq Age Sex Outcome Treatment
1 27 YR Disability