PROPHY-JET POWDER 130002V

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 2010-12-08 for PROPHY-JET POWDER 130002V manufactured by Dentsply Detrey.

Event Text Entries

[1811261] In this event is was reported that five different patients experienced lip swelling and ablation of the oral mucosa after a procedure was performed using prophy-jet powder. No medical intervention was required as a result. Latex gloves were used by the dental professional in these incidents.
Patient Sequence No: 1, Text Type: D, B5


[8807315] While it is unk if the prophy-jet powder used in this case caused or contributed to the patient's symptoms, it is possible as allergic reactions ot 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 results are not available as of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2424472-2010-00120
MDR Report Key1923582
Report Source01,05
Date Received2010-12-08
Date of Report2010-11-10
Date Mfgr Received2010-11-10
Date Added to Maude2010-12-21
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. PHILA. ST., STE. 60 SUSQUEHANNA COMMERCE CENTER W.
Manufacturer CityYORK PA 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178457511
Manufacturer G1DENTSPLY PROFESSIONAL
Manufacturer Street1301 SMILE WAY
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal Code17404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROPHY-JET POWDER
Product CodeKOJ
Date Received2010-12-08
Returned To Mfg2010-11-19
Catalog Number130002V
Lot Number091118
Device Expiration Date2012-06-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY DETREY
Manufacturer AddressKONSTANZ GM


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2010-12-08

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