FDA Adverse Event Malfunction Summary report: N

CLARION

MDR report key: 2063799 · Received April 6, 2011

Report

Report Number
3006556115-2011-00145
Event Type
Malfunction
Date Received
April 6, 2011
Date of Event
March 16, 2011
Report Date
March 16, 2011
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Description of Event or Problem · 1

THE PATIENT REPORTEDLY EXPERIENCED A LOSS OF LOCK WITH HER INTERNAL DEVICE. SURGERY TO EXPLANT THE PATIENT'S DEVICE WILL BE SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CLARION COCHLEAR IMPLANT MCM ADVANCED BIONICS LLC AB-5100R NA

Patients

Seq Age Sex Outcome Treatment
1 13 YR