FDA Adverse Event Injury Summary report: N

CONSERVE(R) TOTAL A-CLASS HEAD

MDR report key: 3252994 · Received July 29, 2013

Report

Report Number
1043534-2013-01204
Event Type
Injury
Date Received
July 29, 2013
Date of Event
December 13, 2012
Report Date
June 28, 2013
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC.
Product Code
JDL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THE EVENT CODE IS ADDRESSED IN THE PACKAGE INSERT. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. THIS IS THE SAME EVENT AS 1043534-2013-01203, 01205, 01206.

Description of Event or Problem · 1

ALLEGEDLY PATIENT WAS REVISED DUE MOM COMPLICATIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352656 CONSERVE(R) TOTAL A-CLASS HEAD HIP COMPONENT, CODE:JDL JDL WRIGHT MEDICAL TECHNOLOGY, INC. 108715115

Patients

Seq Age Sex Outcome Treatment
1 66 YR Required Intervention