LIGHT SOURCE, 500XL, XENON 72200568

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-31 for LIGHT SOURCE, 500XL, XENON 72200568 manufactured by Smith & Nephew, Inc..

Event Text Entries

[81572218] (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[81572219] It was reported that device light started flickering and then blew. After a while wires started to burn or melt, smoke everywhere. No injuries were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1643264-2017-00445
MDR Report Key6753778
Date Received2017-07-31
Date of Report2017-11-10
Date of Event2017-07-21
Date Mfgr Received2017-11-07
Date Added to Maude2017-07-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJAMES GONZALES
Manufacturer Street7000 W. WILLIAM CANNON DR
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street76 S. MERIDIAN AVE.
Manufacturer CityOKLAHOMA CITY OK 731076512
Manufacturer CountryUS
Manufacturer Postal Code731076512
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLIGHT SOURCE, 500XL, XENON
Generic NameLIGHT, SURGICAL, FLOOR STANDING
Product CodeFSS
Date Received2017-07-31
Catalog Number72200568
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address76 S. MERIDIAN AVE. OKLAHOMA CITY OK 731076512 US 731076512


Patients

Patient NumberTreatmentOutcomeDate
10 2017-07-31

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