NUPRO PROPHY PASTE 80132801

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,05 report with the FDA on 2014-11-22 for NUPRO PROPHY PASTE 80132801 manufactured by Dentsply Professional.

Event Text Entries

[17292706] A chemtrec emergency incident report was received that reported a pediatric patient was treated with nupro prophy paste with fluoride and later experienced a rash. There was no report of intervention.
Patient Sequence No: 1, Text Type: D, B5


[17500739] While it is unknown if the device used in this case caused or contributed to the patient's symptoms, it is possible as allergic reactions to dental materials are known and reported, with medical consequences being dependent upon the severity of the individual allergic response and subsequent exposure to the same material. Therefore, this event meets the criteria for reportability per 21 cfr part 803. The device is available for evaluation, though has not been returned as of this report. Evaluation results will be submitted as they become available.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2424472-2014-00011
MDR Report Key4279199
Report Source00,05
Date Received2014-11-22
Date of Report2014-10-17
Date of Event2014-10-16
Date Mfgr Received2014-10-17
Date Added to Maude2014-11-28
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 ContactHELEN LEWIS
Manufacturer StreetSUSQUEHANNA COMMERCE CTR W. 221 W. PHILADELPHIA ST., STE 60
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal17404
Manufacturer Phone7178457511
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNUPRO PROPHY PASTE
Generic NameORAL CAVITY ABRASIVE POLISHING AGENT
Product CodeEJR
Date Received2014-11-22
Catalog Number80132801
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY PROFESSIONAL
Manufacturer AddressYORK PA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-11-22

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