LUXSTAR UNIT MOUNT LIGHT UL1000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2015-05-27 for LUXSTAR UNIT MOUNT LIGHT UL1000 manufactured by Marus.

Event Text Entries

[5916459] A dental professional was performing routine medical treatment to a patient when the lens head shield/holder fell off the marus dental light and hit the patient on the neck causing a slight burn. There was no serious injuries reported.
Patient Sequence No: 1, Text Type: D, B5


[13416583] The lens heat shield/holder from the dental light has a three prong locking mechanism which locks the lens heat shield/holder into place. The lens heat shield/holder has to be removed by the end user when cleaning the lens or replacing the halogen bulb during routine operator maintenance. The installation instructions, use and care instructions, and labeling clearly state to ensure the lens heat shield/holder is properly secure by snapping the part back into place. The light is over 11 years old and is past the expected life of the device.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1017522-2015-00009
MDR Report Key4801706
Report Source05,06
Date Received2015-05-27
Date of Report2015-04-28
Date of Event2015-04-27
Date Mfgr Received2015-04-28
Device Manufacturer Date2003-10-01
Date Added to Maude2015-06-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactFRANK RAY
Manufacturer Street11727 FRUEHAUF DR.
Manufacturer CityCHARLOTTE NC 28273
Manufacturer CountryUS
Manufacturer Postal28273
Manufacturer Phone7045877227
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLUXSTAR UNIT MOUNT LIGHT
Generic NameDENTAL OPERARTING LIGHT
Product CodeEAZ
Date Received2015-05-27
Model NumberUL1000
Catalog NumberUL1000
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMARUS
Manufacturer Address11727 FRUEHAUF DR. CHARLOTTE NC 28273 US 28273


Patients

Patient NumberTreatmentOutcomeDate
10 2015-05-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.