GUTTA-PERCHA PLUGGER A289S00100200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,other report with the FDA on 2020-01-08 for GUTTA-PERCHA PLUGGER A289S00100200 manufactured by Dentsply Maillefer.

Event Text Entries

[178620006] While no serious injury resulted in this event, 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. 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


[178620007] In this event it was reported that a plugger broke during use; no injury resulted and the separated piece has been retrieved.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031010-2019-00287
MDR Report Key9566713
Report SourceFOREIGN,OTHER
Date Received2020-01-08
Date of Report2020-01-01
Date Mfgr Received2019-12-02
Date Added to Maude2020-01-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 MAILLEFER
Manufacturer StreetCHEMIN DU VERGER 3
Manufacturer CityBALLAIGUES, 1338
Manufacturer CountrySZ
Manufacturer Postal Code1338
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGUTTA-PERCHA PLUGGER
Generic NamePLUGGER, ROOT CANAL, ENDODONTIC
Product CodeEKR
Date Received2020-01-08
Model NumberNA
Catalog NumberA289S00100200
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY MAILLEFER
Manufacturer AddressCHEMIN DU VERGER 3 BALLAIGUES, 1338 SZ 1338


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-08

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