FDA Adverse Event Injury Summary report: N

CONSERVE TOTAL HEAD W/BFH

MDR report key: 1030107 · Received April 14, 2008

Report

Report Number
1043534-2008-00065
Event Type
Injury
Date Received
April 14, 2008
Date of Event
March 26, 2008
Report Date
March 22, 2008
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
KWA
PMA / PMN Number
K021349
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION IS NOT COMPLETE. PROD NOT RETURNED FOR EVAL. TRENDS WILL BE EVALUATED. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. ALTHOUGH SEVERAL ATTEMPTS HAVE BEEN MADE, A MEDWATCH 3500A HAS NOT BEEN RECEIVED FROM THE USER FACILITY. THIS IS THE SAME EVENT AS 1043534-2008-00063, 00064, 00066.

Description of Event or Problem · 1

ALLEGEDLY REVISED DUE TO THE REVISION OF A RELATED PROSTHESIS (NECK).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CONSERVE TOTAL HEAD W/BFH KWA WRIGHT MEDICAL TECHNOLOGY, INC. 01461666

Patients

Seq Age Sex Outcome Treatment
1 66 YR Hospitalization| R