FDA Adverse Event Malfunction Summary report: N

HIRES 90K

MDR report key: 2091180 · Received May 11, 2011

Report

Report Number
3006556115-2011-00227
Event Type
Malfunction
Date Received
May 11, 2011
Date of Event
April 21, 2011
Report Date
April 21, 2011
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
AUDIOLOGIST

Narratives

Description of Event or Problem · 1

THE PATIENT WAS REPORTEDLY EXPERIENCING LOSS OF SOUND AND LOSS OF LOCK. EXTERNAL EQUIPMENT WAS EXCHANGED; HOWEVER, THIS DID NOT RESOLVE THE ISSUE. TESTING SHOWED THAT THE DEVICE IS NOT FUNCTIONING. SURGERY TO EXPLANT THE PATIENT'S DEVICE HAS BEEN SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HIRES 90K COCHLEAR IMPLANT MCM ADVANCED BIONICS LLC CI-1400-01 NA

Patients

Seq Age Sex Outcome Treatment
1 7 YR