FDA Adverse Event Malfunction Summary report: N

HIRES 90K IMPLANT

MDR report key: 3983274 · Received July 3, 2014

Report

Report Number
3006556115-2014-00331
Event Type
Malfunction
Date Received
July 3, 2014
Date of Event
June 13, 2014
Report Date
June 13, 2014
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
AUDIOLOGIST
Health Professional
Yes

Narratives

Description of Event or Problem · 1

THE PT REPORTEDLY EXPERIENCED INTERMITTENCIES FOLLOWED BY LOSS OF LOCK. EXTERNAL EQUIPMENT WAS EXCHANGED AND PROGRAMMING ADJUSTMENTS WERE MADE, HOWEVER, THE ISSUE WAS NOT RESOLVED. TESTING REVEALED THE DEVICE IS NON-FUNCTIONING. REVISION SURGERY IS SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
392069 HIRES 90K IMPLANT COCHLEAR IMPLANT MCM ADVANCED BIONICS LLC CI-1400-01 NA

Patients

Seq Age Sex Outcome Treatment
1 12 YR Male