NUPRO PROPHY PASTE 801222

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2015-02-12 for NUPRO PROPHY PASTE 801222 manufactured by Dentsply Professional.

Event Text Entries

[5358999] In this event it was reported that after using nupro prophy paste, a pt experienced an asthmatic episode, which the doctor thinks may be due to an allergy to one of the ingredients in the prophy paste. The pt was able to treat himself with a "spray".
Patient Sequence No: 1, Text Type: D, B5


[12890648] While it is unk if the device used in this case caused or contributed to the pt'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 eval, though has not been returned as of this report. Eval results will be submitted as they become available.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2424472-2015-00003
MDR Report Key4527485
Report Source01,05
Date Received2015-02-12
Date of Report2015-01-13
Date of Event2015-01-04
Date Mfgr Received2015-01-13
Date Added to Maude2015-02-20
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 Street221 W. PHILADELPHIA ST STE 60, SUSQUEHANNA COMMERCE CTR W.
Manufacturer CityYORK PA 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178457511
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNUPRO PROPHY PASTE
Generic NameAGENT, POLISHING, ABRASIVE, ORAL CAV
Product CodeEJR
Date Received2015-02-12
Catalog Number801222
Lot NumberUNK
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. Required No Informationntervention 2015-02-12

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