FDA Adverse Event Malfunction Summary report: N

GREENLIGHT ADDSTAT

MDR report key: 2022074 · Received February 28, 2011

Report

Report Number
2937094-2011-00211
Event Type
Malfunction
Date Received
February 28, 2011
Date of Event
January 25, 2011
Report Date
January 31, 2011
Manufacturer
AMS, INNOVATION CENTER - SILICON VALLEY
Product Code
GEX
PMA / PMN Number
K062719
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY A CUSTOMER ON (B)(6) 2011, THE FIBER FORWARD FIRED AND/OR THE FIBER WAS DAMAGED AT THE TIP AT 31,419 JOULES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMS, INNOVATION CENTER - SILICON VALLEY NA 036H

Patients

Seq Age Sex Outcome Treatment
1 Other