FDA Adverse Event Malfunction Summary report: N

HIRES 90K IMPLANT

MDR report key: 3113269 · Received May 8, 2013

Report

Report Number
3006556115-2013-00184
Event Type
Malfunction
Date Received
May 8, 2013
Date of Event
April 18, 2013
Report Date
April 18, 2013
Manufacturer
ADVANCED BIONICS LLC
Product Code
MCM
PMA / PMN Number
P960058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO
Reporter Occupation
NO INFORMATION

Narratives

Description of Event or Problem · 1

THE PT REPORTEDLY EXPERIENCED INTERMITTENCIES, FOLLOWED BY NO LOCK BETWEEN THE INTERNAL DEVICE AND EXTERNAL EQUIPMENT. PROGRAMMING ADJUSTMENTS HAVE BEEN MADE AND EXTERNAL EQUIPMENT EXCHANGED, HOWEVER THIS DID NOT RESOLVE THE ISSUE. REVISION SURGERY HAS BEEN SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
202194 HIRES 90K IMPLANT COCHLEAR IMPLANT MCM ADVANCED BIONICS LLC CI-1400-01 NA

Patients

Seq Age Sex Outcome Treatment
1 5 YR