GUTTA-PERCHA PLUGGER A289S00100200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-17 for GUTTA-PERCHA PLUGGER A289S00100200 manufactured by Dentsply Maillefer.

Event Text Entries

[117847251] 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 is available for evaluation, though results are not available as of this report. Evaluation results will be submitted as they become available.
Patient Sequence No: 1, Text Type: N, H10


[117847252] In this event it was reported that a plugger broke during use; no injury resulted and the separated piece was retrieved.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8031010-2018-00083
MDR Report Key7793542
Date Received2018-08-17
Date of Report2018-08-28
Date Mfgr Received2018-08-20
Date Added to Maude2018-08-17
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 MAILLEFER
Manufacturer StreetCHEMIN DU VERGER 3
Manufacturer CityBALLAIGUES, 1338
Manufacturer CountrySZ
Manufacturer Postal Code1338
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameGUTTA-PERCHA PLUGGER
Generic NamePLUGGER, ROOT CANAL, ENDODONTIC
Product CodeEKR
Date Received2018-08-17
Returned To Mfg2018-08-07
Model NumberNA
Catalog NumberA289S00100200
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY MAILLEFER
Manufacturer AddressCHEMIN DU VERGER 3 BALLAIGUES, 1338 SZ 1338


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-17

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