FDA Adverse Event Injury Summary report: N

CLARION

MDR report key: 374998 · Received February 1, 2002

Report

Report Number
2029203-2002-00029
Event Type
Injury
Date Received
February 1, 2002
Date of Event
October 1, 1999
Report Date
January 31, 2002
Manufacturer
ADVANCED BIONICS CORPORATION
Product Code
MCM
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IN 1999, PATIENT REPORTED PAIN OVER SKIN FLAP AT THE IMPLANT SITE. THERE WERE NO REPORTS OF ICS PERFORMANCE PROBLEMS PRIOR TO DEVICE EXPLANTATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CLARION COCHLEAR IMPLANT MCM ADVANCED BIONICS CORPORATION MMT-5100L NA

Patients

Seq Age Sex Outcome Treatment
1 72 YR Required Intervention