GREENLIGHT MOXY FIBER OPTIC
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
(B)(4).
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.
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 |