PROFILE GT ROTARY INSTRUMENT GTR0602025

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2005-11-15 for PROFILE GT ROTARY INSTRUMENT GTR0602025 manufactured by Dentsply Tulsa.

Event Text Entries

[405904] It was reported that a file separated in a canal containing a fractured root (the fracture was present prior to initiation of procedure). The tooth was ultimately extracted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2320721-2005-00479
MDR Report Key646362
Report Source05
Date Received2005-11-15
Date of Report2005-10-26
Date of Event2005-10-25
Date Mfgr Received2005-10-26
Device Manufacturer Date2005-07-01
Date Added to Maude2005-11-18
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 Location0
Manufacturer ContactDR PATRICIA KIHN
Manufacturer StreetSUUQUEHANNA COMMERCE CENTER W 221 W PHILA ST STE 60
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal17404
Manufacturer Phone7178457511
Manufacturer G1DENTSPLY TULSA
Manufacturer Street608 ROLLING HILLS DRIVE
Manufacturer CityJOHNSON CITY TN 37604
Manufacturer CountryUS
Manufacturer Postal Code37604
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePROFILE GT ROTARY INSTRUMENT
Generic NameDENTAL FILE
Product CodeEMR
Date Received2005-11-15
Returned To Mfg2005-11-02
Model NumberNA
Catalog NumberGTR0602025
Lot Number071805004
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key635867
ManufacturerDENTSPLY TULSA
Manufacturer Address* JOHNSON CITY TN * US
Baseline Brand NamePROFILE GT ROTARY INSTRUMENT
Baseline Generic NameDENTAL FILE
Baseline Model NoNA
Baseline Catalog NoGTR0602025
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2005-11-15

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