FDA Adverse Event Malfunction Summary report: N

GREENLIGHT MOXY FIBER OPTIC

MDR report key: 2915390 · Received January 9, 2013

Report

Report Number
2937094-2013-00045
Event Type
Malfunction
Date Received
January 9, 2013
Date of Event
January 18, 2012
Report Date
January 26, 2012
Manufacturer
AMERICAN MEDICAL SYSTEMS
Product Code
GEX
PMA / PMN Number
K100746
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

THE COMPONENT CODES FIBER AND CAP REFER TO THE RESULT CODE THERMAL PROBLEM. ANALYSIS: THE FIBER WAS FOUND TO HAVE A CIRCUMFERENTIAL FRACTURE OF THE GLASS CAP, PROXIMAL TO THE FIBER/CAP FUSION ZONE; THE FIBER PROXIMAL TO THE FRACTURE WAS FOUND TO ROTATE INDEPENDENTLY OF THE METAL CAP. BURNT ON DETRITUS AND DEVITRIFICATION OF THE CAP OUTPUT WINDOW WAS ALSO OBSERVED. THE FIBER CONDITION WOULD LIKELY RESULT IN ACTIVATION OF THE SYSTEM'S FIBERLIFE FUNCTION WHICH WILL MODULATE (PULSE) THE OUTPUT BEAM, RESULTING IN REDUCED TISSUE VAPORIZATION EFFICIENCY AND/OR SEND THE SYSTEM TO STANDBY MODE. THE FIBER/CAP CONDITION COULD ALSO RESULT IN FORWARD FIRING CONDITION OF THE SIDE-FIRING SURGICAL FIBER. THE ROOT CAUSE OF THE DEVICE FAILURE WAS DETERMINED TO BE HEAT ACCUMULATION DUE TO TISSUE CONTACT AND/OR ANATOMICAL/PROCEDURAL FACTORS ENCOUNTERED DURING THE PROCEDURE, RESULTING IN FIBER BREAKAGE AND CAP DAMAGE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE TIP OF THE SURGICAL FIBER WAS DAMAGED AT 220,000 JOULES OF USE DURING A PROSTATE PROCEDURE. THE CASE WAS COMPLETED BY TURP. THERE WAS NO REPORT OF PT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
12623 GREENLIGHT MOXY FIBER OPTIC POWERED SURGICAL LASER INSTRUMENT GEX AMERICAN MEDICAL SYSTEMS 10-2400 141A

Patients

Seq Age Sex Outcome Treatment
1 Other ACCESSORIES| GREENLIGHT XPS LASER SYSTEM