NUPRO PROPHY PASTE 801329

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2015-06-18 for NUPRO PROPHY PASTE 801329 manufactured by Dentsply Professional.

Event Text Entries

[19347763] In this event it was reported that a pediatric patient with many allergies, experienced nausea and vomiting following treatment with nupro prophy paste (chocolate bliss flavor). The patient's mother was sent a list of ingredients in order to have allergy testing done. Results are not available as of this report.
Patient Sequence No: 1, Text Type: D, B5


[19627214] 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 was not returned for evaluation and the lot number was not provided for retained-product testing and/or dhr review.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2424472-2015-00034
MDR Report Key4860132
Report Source05
Date Received2015-06-18
Date of Report2015-05-22
Date Mfgr Received2015-05-22
Date Added to Maude2015-06-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA0
Event Location0
Manufacturer ContactHELEN LEWIS
Manufacturer Street221 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 Received2015-06-18
Catalog Number801329
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY PROFESSIONAL
Manufacturer AddressYORK PA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-06-18

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