FDA Adverse Event Malfunction Summary report: N

HIRES 90K

MDR report key: 1920732 · Received October 29, 2010

Report

Report Number
3006556115-2010-00522
Event Type
Malfunction
Date Received
October 29, 2010
Date of Event
October 8, 2010
Report Date
October 8, 2010
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
AUDIOLOGIST

Narratives

Description of Event or Problem · 1

THE PT REPORTEDLY EXPERIENCED SOUND QUALITY ISSUES. EXTERNAL EQUIPMENT WAS EXCHANGED AND PROGRAMMING ADJUSTMENT WERE MADE, HOWEVER, THIS DID NOT RESOLVE THE ISSUE. SURGERY TO EXPLANT THE PT'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 83 YR