SVCE REPL LIGHT SOURCE 500XL XENON 72200568S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-05-09 for SVCE REPL LIGHT SOURCE 500XL XENON 72200568S manufactured by Smith & Nephew, Inc..

Event Text Entries

[144549680] .
Patient Sequence No: 1, Text Type: N, H10


[144549681] It was reported that the device was overheating. No patient was involved as the failure was found before the surgery.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1643264-2019-00326
MDR Report Key8594621
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-05-09
Date of Report2019-06-28
Date of Event2019-04-30
Date Mfgr Received2019-06-26
Date Added to Maude2019-05-09
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 ContactJIM GONZALES
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123585706
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 Report3

Device Details

Brand NameSVCE REPL LIGHT SOURCE 500XL XENON
Generic NameIMAGE, ILLUMINATION, FIBEROPTIC, FOR ENDOSCOPE
Product CodeFFS
Date Received2019-05-09
Returned To Mfg2019-05-08
Catalog Number72200568S
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
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 2019-05-09

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