FDA Adverse Event Injury Summary report: N

CONSERVE(R) TOTAL A-CLASS HEAD

MDR report key: 6043226 · Received October 20, 2016

Report

Report Number
3010536692-2016-01299
Event Type
Injury
Date Received
October 20, 2016
Report Date
September 21, 2016
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
JDL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ALLEGEDLY, THE PATIENT WAS REVISED DUE TO THE FOLLOWING MOM COMPLICATIONS; HIP SOCKET PAIN. ADDITIONAL INFORMATION RECEIVED. ALLEGEDLY, THE PATIENT WILL BE REVISED ON (B)(6) 2016.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
695632 CONSERVE(R) TOTAL A-CLASS HEAD HIP COMPONENT JDL MICROPORT ORTHOPEDICS INC. 085246822

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention