K?R DESENSITIZER 10-1012

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-04-03 for K?R DESENSITIZER 10-1012 manufactured by Evolve Dental Technologies, Inc..

Event Text Entries

[104219313] Likely allergic reaction to the hema in the desensitizer.
Patient Sequence No: 1, Text Type: N, H10


[104219314] Dentist reported that patient's lips are swollen after whitening. Advised dentist to inform the patient to discontinue use of the k? R desensitizer permanently, and if need be, she can see her general practitioner to help with any symptoms. Followed with dental office several times, office did not have patient status to report.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010407924-2018-00011
MDR Report Key7393689
Report SourceHEALTH PROFESSIONAL
Date Received2018-04-03
Date of Report2018-02-26
Date of Event2018-02-26
Date Mfgr Received2018-02-26
Date Added to Maude2018-04-03
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 FDA3
Event Location3
Manufacturer ContactMS. LISA FJASTAD
Manufacturer Street5 VANDERBILT
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9497130909
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameK?R DESENSITIZER
Generic NameAGENT, TOOTH BONDING, RESIN
Product CodeKLE
Date Received2018-04-03
Catalog Number10-1012
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEVOLVE DENTAL TECHNOLOGIES, INC.
Manufacturer Address5 VANDERBILT IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening 2018-04-03

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