FDA Adverse Event Injury Summary report: N

CONSERVE(R) TOTAL A-CLASS HEAD

MDR report key: 3922327 · Received July 9, 2014

Report

Report Number
3010536692-2014-00974
Event Type
Injury
Date Received
July 9, 2014
Date of Event
July 8, 2013
Report Date
June 12, 2014
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
JDL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THIS IS THE SAME EVENT AS 3010536692-2014-00972, -00973, 00975, 00976. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE.

Description of Event or Problem · 1

ALLEGEDLY THE PATIENT WAS REVISED DUE TO DISLOCATION (LEFT).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
400071 CONSERVE(R) TOTAL A-CLASS HEAD HIP COMPONENT JDL MICROPORT ORTHOPEDICS INC. 1402518

Patients

Seq Age Sex Outcome Treatment
1 47 YR Required Intervention