FDA Adverse Event Malfunction Summary report: N

HIRES 90K

MDR report key: 1051593 · Received May 19, 2008

Report

Report Number
3006556115-2008-00237
Event Type
Malfunction
Date Received
May 19, 2008
Date of Event
April 21, 2008
Report Date
April 21, 2008
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
AUDIOLOGIST

Narratives

Description of Event or Problem · 1

THE PT REPORTEDLY EXPERIENCED INTERMITTENCIES WITH HER INTERNAL DEVICE FOLLOWED BY A LOSS OF LOCK. EXTERNAL EQUIPMENT WAS EXCHANGED, HOWEVER, THIS DID NOT RESOLVE THE PROBLEM. SURGERY TO EXPLANT THE PT'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-1400-01 NA

Patients

Seq Age Sex Outcome Treatment
1