FDA Adverse Event Malfunction Summary report: N

GREENLIGHT ADDSTAT

MDR report key: 2030393 · Received March 7, 2011

Report

Report Number
2937094-2011-00325
Event Type
Malfunction
Date Received
March 7, 2011
Date of Event
November 29, 2010
Report Date
December 1, 2010
Manufacturer
AMS INNOVATION CENTER - SILICON VALLEY
Product Code
GEX
PMA / PMN Number
K062719
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE EVENT DESCRIPTION THE CUSTOMER REPORTED TO AMS DID NOT INDICATE A POTENTIAL PT SAFETY ISSUE. THE DEVICE WAS SUBSEQUENTLY RETURNED TO AMS AND ANALYZED. THE INFO FROM THIS FAILURE ANALYSIS WAS RECEIVED ON (B)(6) 2011 AND THE RESULTS OF THE FAILURE ANALYSIS INDICATED THAT AN MDR WAS REQUIRED. THE FAILURE ANALYSIS DISCLOSED THAT THE FIBER CAP WAS WORN OUT. THE FIBER CAP WAS INTACT AND STILL ATTACHED, THE FIBER CAP WAS DRILLED THROUGH. THE FIBER CAP EXHIBITED ANY OR ALL OF CHAR, DEVITRIFICATION, CRATER AND MELTED GLASS. THE NORMAL WEAR OUT MAY BE ACCELERATED BY TECHNIQUE CAUSING A LACK OF COOLING. THE ROOT CAUSE OF THE DEVICE FAILURE WAS DETERMINED TO BE USE AND ACCELERATED BY TISSUE CONTACT. THE PRODUCT LABELING (PRODUCT INSERT 0127-1410) WARNS THAT TISSUE CONTACT OR TISSUE PROBING MAY CAUSE FIBER DAMAGE OR BREAKAGE. THE PRODUCT LABELING ALSO WARNS OF POSSIBLE CAP DETACHMENT IN THE PT AND INSTRUCTIONS FOR RETRIEVING.

Description of Event or Problem · 1

IT WAS REPORTED BY A CUSTOMER ON (B)(6) 2010, THERE WAS A DECREASE IN FIBER VAPORIZATION EFFICIENCY AT 50,000 JOULES. A FAILURE ANALYSIS, CONDUCTED BY AN AMERICAN MEDICAL SYSTEMS QUALITY ENGINEER, DISCLOSED THAT THE FIBER CAP WAS WORN OUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMS INNOVATION CENTER - SILICON VALLEY NA 028H

Patients

Seq Age Sex Outcome Treatment
1 Other