AH PLUS JET 60620115

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2016-07-06 for AH PLUS JET 60620115 manufactured by Dentsply Detrey Gmbh.

Event Text Entries

[48918335] 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


[48918336] It was reported that a patient experienced severe pain after having endodontic treatment that included ah plus. The patient was tested for allergies and it was discovered that the patient is allergic to ah plus.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010638-2016-00002
MDR Report Key5773404
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2016-07-06
Date of Report2016-06-06
Date Mfgr Received2016-06-06
Date Added to Maude2016-07-06
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 ContactMRS. HELEN LEWIS
Manufacturer Street221 W. PHILADELPHIA ST. SUITE 60W
Manufacturer CityYORK PA 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178494229
Manufacturer G1DENTSPLY DETREY GMBH
Manufacturer StreetDETREY STRASSE 1
Manufacturer CityKONSTANZ, 78467
Manufacturer CountryGM
Manufacturer Postal Code78467
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAH PLUS JET
Generic NameRESIN, ROOT CANAL FILLING
Product CodeKIF
Date Received2016-07-06
Model NumberNA
Catalog Number60620115
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY DETREY GMBH
Manufacturer AddressDETREY STRASSE 1 KONSTANZ, 78467 GM 78467


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-07-06

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