GREENLIGHT ADDSTAT
Report
- Report Number
- 2937094-2011-00558
- Event Type
- Malfunction
- Date Received
- April 6, 2011
- Date of Event
- May 29, 2010
- Report Date
- September 16, 2010
- Manufacturer
- AMS 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
THE EVENT DESCRIPTION THE CUSTOMER REPORTED TO AMS DID NOT INDICATE A POTENTIAL PATIENT SAFETY ISSUE. THE DEVICE WAS SUBSEQUENTLY RETURNED TO AMS AND ANALYZED. THE INFORMATION FROM THIS FAILURE ANALYSIS WAS RECEIVED ON (B)(4) 2011 AND THE RESULTS OF THE FAILURE ANALYSIS INDICATED THAT AN MDR WAS REQUIRED. THE FAILURE ANALYSIS DISCLOSED THAT THE FIBER CAP WAS WORN OUT. THE FIBER CAP WAS INTACT AND STILL ATTACHED. THE FIBER CAP WAS DRILLED THROUGH. THE FIBER CAP EXHIBITED ANY OR ALL OF CHAR, DEVITRIFICATION, CRATER, MELTED GLASS AND MINOR BEVEL MELTING. THE NORMAL WEAR OUT MAY BE ACCELERATED BY TECHNIQUE CAUSING A LACK OF COOLING. THE ROOT CAUSE OF THE DEVICE FAILURE WAS DETERMINED TO BE USE AND ACCELERATED BY TISSUE CONTACT. THE PRODUCT LABELING (PRODUCT INSERT 0127-1410) WARNS THAT TISSUE CONTACT OR TISSUE PROBING MAY CAUSE FIBER DAMAGE OR BREAKAGE. THE PRODUCT LABELING ALSO WARNS OF POSSIBLE CAP DETACHMENT IN THE PATIENT AND INSTRUCTIONS FOR RETRIEVING.
IT WAS REPORTED BY A CUSTOMER ON (B)(4) 2010 THERE WAS DIMINISHED FIBER VAPORIZATION; THE FIBER BEAM WAS VERY LIGHT AND DID NOT VAPORIZE THE TISSUE VERY WELL AT 18,396 JOULES. A FAILURE ANALYSIS, CONDUCTED BY AN AMERICAN MEDICAL SYSTEMS QUALITY ENGINEER, DISCLOSED THAT THE FIBER CAP WAS WORN OUT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GREENLIGHT ADDSTAT | SURGICAL FIBER | GEX | AMS INNOVATION CENTER-SILICON VALLEY | NA | 914K |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |