FDA Adverse Event Malfunction Summary report: N

GREENLIGHT MOXY FIBER OPTIC

MDR report key: 3931819 · Received July 14, 2014

Report

Report Number
2937094-2014-00617
Event Type
Malfunction
Date Received
July 14, 2014
Date of Event
July 3, 2014
Report Date
July 7, 2014
Manufacturer
AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)
Product Code
GEX
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

PRODUCT EVALUATION: FAILURE ANALYSIS FOR FIBER (B)(4): THE FIBER SHOWS A CIRCUMFERENTIAL FRACTURE DISTAL TO FIBER/CAP FUSION ZONE AT THE BEVEL EDGE; THE FIBER PROXIMAL TO FRACTURE CAN ROTATE INDEPENDENTLY OF METAL CAP; THE GLASS CAP EXHIBITS MODERATE DEVITRIFICATION; THE METAL CAP EXHIBITS MILD DETRITUS ADHESION. BASED ON THE ANALYSIS ABOVE, THE POTENTIAL FOR FORWARD FIRING MAY EXIST. PROBABLE ROOT CAUSE: BASED ON THE PRODUCT ANALYSIS RESULTS, THE PROBABLE ROOT CAUSE OF THE FAILURE IS: HEAT ACCUMULATION. CAP WEAR WAS ACCELERATED DUE TO ANATOMICAL/PROCEDURAL FACTORS (TISSUE CONTACT AND TECHNIQUE) ENCOUNTERED DURING THE PROCEDURE WHICH WOULD LIMIT THE PERFORMANCE OF THE FIBER.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A PROSTATE PROCEDURE, THE FIRST FIBER ISSUE ¿END FIRING". THE FIBER WAS EXCHANGED; THE SECOND FIBER ISSUE ¿END FIRING" ADDITIONAL INFORMATION: USED 2 FIBER CARDS DUE TO POWER ISSUES. THE FIBER WAS EXCHANGED; THE THIRD FIBER ISSUE ¿END FIRING". THE FIBER WAS EXCHANGED, THE FOURTH FIBER ISSUE "END FIRING". THE FIBER WAS EXCHANGED; THE FIFTH FIBER ISSUE "END FIRING". THE FIBER WAS EXCHANGED; AND THE CASE COMPLETED. PATIENT OUTCOME: "OK" REPORTED. THIS REPORT IS FOR THE 5TH FIBER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
411344 GREENLIGHT MOXY FIBER OPTIC POWERED LASER SURGICAL INSTRUMENT GEX AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE) 0010-2400 402A

Patients

Seq Age Sex Outcome Treatment
1