AH PLUS ROOT CANAL SEALER 606.20.112

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-07 for AH PLUS ROOT CANAL SEALER 606.20.112 manufactured by Dentsply Detrey Gmbh.

Event Text Entries

[137559029] There has been a previous report received where this malfunction resulted in a serious injury. Therefore, it must be presumed that recurrence of this malfunction could possibly cause or contribute to a serious injury or require medical or surgical intervention to preclude such. As such, this event is reportable per 21cfr part 803. Multiple unsuccessful attempts were made to obtain the device for evaluation. A dhr review was conducted with no discrepancies noted.
Patient Sequence No: 1, Text Type: N, H10


[137559030] It was reported that a package of ah plus contained two tubes of the same paste. There was no report of injury to the patient and no report of medical/surgical intervention resulting from use of this product as the problem was apparently discovered before use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010638-2019-00001
MDR Report Key8315720
Date Received2019-02-07
Date of Report2019-02-07
Date Mfgr Received2019-01-09
Date Added to Maude2019-02-07
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 ContactMR. KARL NITTINGER
Manufacturer Street221 W. PHILADELPHIA ST. SUITE 60W
Manufacturer CityYORK PA 17401
Manufacturer CountryUS
Manufacturer Postal17401
Manufacturer Phone7178494424
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 Report0

Device Details

Brand NameAH PLUS ROOT CANAL SEALER
Generic NameRESIN, ROOT CANAL FILLING
Product CodeKIF
Date Received2019-02-07
Model NumberNA
Catalog Number606.20.112
Lot Number1709000825
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
10 2019-02-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.