GREENLIGHT ADDSTAT
Report
- Report Number
- 2937094-2011-01055
- Event Type
- Malfunction
- Date Received
- May 17, 2011
- Date of Event
- November 23, 2010
- Report Date
- February 15, 2011
- Manufacturer
- AMS, INNOVATION CENTER - SILICON VALLEY
- Product Code
- GEX
- PMA / PMN Number
- K062719
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- ID, 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 INFO FROM THIS FAILURE ANALYSIS WAS RECEIVED ON (B)(6) 2011 AND THE RESULTS OF THE FAILURE ANALYSIS INDICATED THAT AN MDR WAS REQUIRED. THE FAILURE ANALYSIS DISCLOSED THAT THE FIBER CAP REGION BURNED AND MELTED, THE CAP REMAINED INTACT AND ATTACHED. THE FIBER CAP WAS DRILLED THROUGH. THE FIBER JACKET STARTED TO MELT. THE FIBER CAP EXHIBITED DEVITRIFICATION, CRATER AND MELTED GLASS. THE ROOT CAUSE OF THE DEVICE FAILURE WAS DETERMINED TO BE HEAT ACCUMULATION. THE PRODUCT LABELING (PRODUCT INSERT (B)(4)) WARNS THAT TISSUE CONTACT OR TISSUE PROBING MAY CAUSE FIBER DAMAGE OR BREAKAGE. THE PRODUCT LABELING ALSO WARNS OF POSSIBLE CAP DETACHMENT IN THE PT AND INSTRUCTIONS FOR RETRIEVING.
IT WAS REPORTED BY A CUSTOMER ON (B)(6) 2010 THERE WAS SIGNIFICANTLY DIMINISHED FIBER VAPORIZATION EFFICIENCY AT 73,308 JOULES. A FAILURE ANALYSIS, CONDUCTED BY AN AMERICAN MEDICAL SYSTEMS QUALITY ENGINEER, DISCLOSED THAT THE FIBER CAP REGION BURNED AND MELTED, THE CAP REMAINED INTACT AND ATTACHED. THE FIBER CAP WAS DRILLED THROUGH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GREENLIGHT ADDSTAT | SURGICAL FIBER | GEX | AMS, INNOVATION CENTER - SILICON VALLEY | NA | 847T |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |