MPOWER TWO TRIGGER MODULAR HANDPIECE PRO6202

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01,06,07 report with the FDA on 2007-12-04 for MPOWER TWO TRIGGER MODULAR HANDPIECE PRO6202 manufactured by Conmed Linvatec.

Event Text Entries

[20920642] The handpiece was returned for service with the report that it would work alone. There was no report of injury or surgical delay associated with this event.
Patient Sequence No: 1, Text Type: D, B5


[21198383] No medwatch form received from the user facility. All sections on this form completed by the manufacture. Attempts to obtain further info regarding this event were unsuccessful. Investigation: the handpiece was received for evaluation. During testing of this handpiece, it was found to have the potential to operate in the safe mode related to controller failure. An investigation for this failure mode remains in process. Conmed linvatec will continue to monitor this handpiece for failures.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1017294-2007-00818
MDR Report Key960273
Report Source00,01,06,07
Date Received2007-12-04
Date of Report2007-11-07
Date Mfgr Received2007-11-07
Device Manufacturer Date2004-11-01
Date Added to Maude2008-03-21
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 FDA0
Event Location0
Manufacturer ContactBEVERLY SCHANER
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO FL 33773
Manufacturer CountryUS
Manufacturer Postal33773
Manufacturer Phone7273995169
Manufacturer G1CONMED LINVATEC
Manufacturer Street11311 CONCEPT BLVD.
Manufacturer CityLARGO FL 33773
Manufacturer CountryUS
Manufacturer Postal Code33773
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMPOWER TWO TRIGGER MODULAR HANDPIECE
Generic NameBATTERY HANDPIECE
Product CodeFCO
Date Received2007-12-04
Returned To Mfg2007-11-08
Model NumberNA
Catalog NumberPRO6202
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key965168
ManufacturerCONMED LINVATEC
Manufacturer AddressLARGO FL US


Patients

Patient NumberTreatmentOutcomeDate
10 2007-12-04

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