FDA Adverse Event Malfunction Summary report: N

HIRES 90K

MDR report key: 2231622 · Received August 22, 2011

Report

Report Number
3006556115-2011-00400
Event Type
Malfunction
Date Received
August 22, 2011
Date of Event
August 1, 2011
Report Date
August 1, 2011
Manufacturer
ADVANCED BIONICS, LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE PATIENT REPORTEDLY EXPERIENCED LOSS OF SOUND. EXTERNAL EQUIPMENT WAS EXCHANGED; HOWEVER, THIS DID NOT RESOLVE THE ISSUE. SURGERY TO EXPLANT THE PATIENT'S DEVICE WILL BE SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HIRES 90K COCHLEAR IMPLANT MCM ADVANCED BIONICS, LLC CI-1400-02H NA

Patients

Seq Age Sex Outcome Treatment
1 13 YR