FDA Adverse Event Malfunction Summary report: N

INTRALASE FS2 LASER

MDR report key: 2033105 · Received February 28, 2011

Report

Report Number
3006695864-2011-00013
Event Type
Malfunction
Date Received
February 28, 2011
Date of Event
July 14, 2009
Report Date
February 28, 2011
Manufacturer
AMO MANUFACTURING USA LLC
Product Code
HNO
PMA / PMN Number
K060372
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE: (ISSUES ASSOCIATED WITH THE COMBUSTION OF DEVICE COMPONENTS, RESULTING IN ANY OF THE FOLLOWING: LIGHT, FLAME, SMOKE). AT THE TIME OF THIS REPORT THE UPS HAS NOT BEEN AVAILABLE FOR INVESTIGATION. INFORMATION REGARDING THE RESULTS AND CONCLUSION OF THE PART EVALUATION WILL BE PROVIDED IN A SUPPLEMENTAL MDR. FEEDBACK FROM POWERVAR (UPS SUPPLIER) ON THIS ISSUE: BY ITS VERY NATURE, THE UPM WILL PROVIDE HIGH VOLTAGES AND HIGH CURRENTS NECESSARY TO PROVIDE THE UNINTERRUPTED POWER TO THE SYSTEM. IT IS LIKELY THAT, DUE TO THESE HIGH POWER LEVELS WITHIN THE UNITS, THAT ANY COMPONENT FAILURE WOULD RESULT IN THE DESTRUCTION OF THAT COMPONENT, WHICH MAY RESULT IN HEAT AND/OR SMOKE BEING MOMENTARILY GENERATED. HOWEVER, THE UNIT IS DESIGNED SO THAT THERE IS NO RISK OF FIRE, WITH THE FAULT BEING CONTAINED WITHIN THE ENCLOSURE, SAFETY MECHANISMS TO DISCONNECT THE BATTERY POWER, AND MATERIALS THAT ARE SELF EXTINGUISHING. LASER WAS CHECKED BY A FIELD SERVICE ENGINEER AND PREVENTATIVE MAINTENANCE WAS COMPLETED. LASER WAS OK.

Description of Event or Problem · 1

INTRALASE LASER FS2 IS USED WITH AN UNINTERRUPTIBLE POWER SUPPLY (B)(4). ON (B)(6) 2009 ACCOUNT REPORTED PROBLEMS WITH THE UPS. THE FIELD SERVICE ENGINEER REPORTED THAT DURING SERVICE VISIT SPARKS AND SMOKE WERE OBSERVED FROM THE UPS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INTRALASE FS2 LASER HNO AMO MANUFACTURING USA LLC 20005K

Patients

Seq Age Sex Outcome Treatment
1 UNK Other