FDA Adverse Event Malfunction Summary report: N

GREENLIGHT HPS BPH FIBER OPTIC

MDR report key: 3042265 · Received April 1, 2013

Report

Report Number
2937094-2013-00417
Event Type
Malfunction
Date Received
April 1, 2013
Date of Event
October 31, 2012
Report Date
November 8, 2012
Manufacturer
AMERICAN MEDICAL SYSTEMS
Product Code
GEX
PMA / PMN Number
K062719
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

REFERENCE MFR REPORT #: 2937094-2013-00416. FIBER ANALYSIS: THE GLASS CAP WAS FOUND TO BE FRACTURED AND PARTIALLY BROKEN; GLASS CAP IS FRACTURED DISTAL TO GLUE ZONE. BROKEN AND MELTED BEVEL AREA, BURNT GLUE ON BEVEL PORTION IS EVIDENT. THERE WAS NO INDICATION OR REPORT OF ANY PART OF THE DEVICE REMAINING INSIDE THE PT. THE FIBER CONDITION COULD RESULT IN A FORWARD FIRING CONDITION OF THE SIDE-FIRING SURGICAL FIBER. THE MOST PROBABLE ROOT CAUSE THAT CONTRIBUTED TO THIS FAILURE WAS SUSPECTED TO BE LOCALIZED HEAT ACCUMULATION DUE TO ANATOMICAL/PROCEDURAL FACTORS ENCOUNTERED DURING THE PROCEDURE; CAP WEAR WAS ACCELERATED LIMITED THE PERFORMANCE OF THE FIBER.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A PROSTATE PROCEDURE, A "FIBER PORT OVERHEATED MESSAGE" WAS REC'D AT 20 JOULES OF USE; THE FIBER WAS REPLACED AND THE PROCEDURE CONTINUED USING A SECOND FIBER. AT 90,237 JOULES OF USE, A PROSTATE STONE WAS HIT, RESULTING IN DAMAGE TO THE FIBER TIP; THE SECOND FIBER WAS REPLACED AND THE CASE WAS COMPLETED USING A THIRD FIBER. PT OUTCOME: "NO PT INJURY, OUTCOME OF PT WAS FINE." THIS REPORT IS FOR THE SECOND FIBER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
131946 GREENLIGHT HPS BPH FIBER OPTIC POWERED SURGICAL LASER INSTRUMENT GEX AMERICAN MEDICAL SYSTEMS 10-2090 216H

Patients

Seq Age Sex Outcome Treatment
1