FDA Adverse Event Malfunction Summary report: N

LENSAR LASER SYSTEM-FS 3D

MDR report key: 5116056 · Received October 1, 2015

Report

Report Number
3009026057-2015-00036
Event Type
Malfunction
Date Received
October 1, 2015
Date of Event
July 3, 2015
Report Date
September 30, 2015
Manufacturer
LENSAR, INC
Product Code
OOE
PMA / PMN Number
K120214
Removal / Correction Number
N/A
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AU
Reporter Occupation
SERVICE PERSONNEL

Narratives

Additional Manufacturer Narrative · 1

THE LENSAR FSE REMOVED THE COVER TO THE PSU AND FOUND A DAMAGED/BURNED WIRE THAT PROVIDES POWER TO THE PC THAT IS INTERNAL TO THE PSU. THE ROOT CAUSE FOR THE BURNED WIRE IS THE SATA POWER SUPPLY CONNECTOR ON THE HARD DISK. IT IS MOST LIKELY THAT A SHORT CIRCUIT OCCURRED DIRECTLY IN THE CONNECTOR HOUSING. THIS ASSUMPTION WAS CONFIRMED.

Additional Manufacturer Narrative · 1

THE LENSAR FSE REMOVED THE COVER TO THE PSU AND FOUND A DAMAGED/BURNED WIRE THAT PROVIDES POWER TO THE PC THAT IS INTERNAL TO THE PSU. THE ROOT CAUSE FOR THE BURNED WIRE IS THE SATA POWER SUPPLY CONNECTOR ON THE HARD DISK. IT IS MOST LIKELY THAT A SHORT CIRCUIT OCCURRED DIRECTLY IN THE CONNECTOR HOUSING. THIS ASSUMPTION WAS CONFIRMED.

Description of Event or Problem · 1

A LENSAR DISTRIBUTOR FSE REPORTED THAT THERE WAS A BURNING SMELL AND SMOKE COMING FROM THE SYSTEM. THE SYSTEM WAS ON AND IN THE READY MODE, BUT WAS NOT BEING USED AT THAT TIME. THE SMOKE CAUSED THE FIRE ALARM TO ACTIVATE. THE SYSTEM WAS SHUT OFF, DISCONNECTED AND MOVED FROM THE ROOM.

Description of Event or Problem · 1

A LENSAR DISTRIBUTOR FSE REPORTED THAT THERE WAS A BURNING SMELL AND SMOKE COMING FROM THE SYSTEM. THE SYSTEM WAS ON AND IN THE READY MODE, BUT WAS NOT BEING USED AT THAT TIME. THE SMOKE CAUSED THE FIRE ALARM TO ACTIVATE. THE SYSTEM WAS SHUT OFF, DISCONNECTED AND MOVED FROM THE ROOM

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
652098 LENSAR LASER SYSTEM-FS 3D LENSAR LASER SYSTEM-FS 3D OOE LENSAR, INC 70-00013-001 N/A

Patients

Seq Age Sex Outcome Treatment
1