FDA Adverse Event Malfunction Summary report: N

GREENLIGHT ADDSTAT

MDR report key: 2030620 · Received March 9, 2011

Report

Report Number
2937094-2011-00368
Event Type
Malfunction
Date Received
March 9, 2011
Date of Event
August 19, 2010
Report Date
September 15, 2010
Manufacturer
AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY
Product Code
GEX
PMA / PMN Number
K062719
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, 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 REC'D 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 FRACTURED AND PARTIALLY BROKE OFF. THE FIBER INCLUDED A BROKEN OR MELTED BEVELED AREA. PART OF THE FIBER CAP BROKE OFF; THE ENTIRE FIBER CAP SLID OFF. BURNT GLUE ON THE BEVEL PORTION OF THE FIBER WAS GENERALLY EVIDENT. THIS DEVICE FAILURE IS ASSOCIATED WITH A LACK OF COOLING. THE ROOT CAUSE OF THE DEVICE FAILURE WAS DETERMINED TO BE TISSUE CONTACT AND EMBEDMENT. THE PRODUCT LABELING (PRODUCT INSERT (B)(4)) 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 10,711 JOULES. A FAILURE ANALYSIS, CONDUCTED BY AN AMERICAN MEDICAL SYSTEMS QUALITY ENGINEER, DISCLOSED THAT THE FIBER CAP FRACTURED AND PARTIALLY BROKE OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY NA 020H

Patients

Seq Age Sex Outcome Treatment
1 Other