CAVITRON PLUS PACKAGE G136 8161425

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-07 for CAVITRON PLUS PACKAGE G136 8161425 manufactured by Dentsply Llc.

Event Text Entries

[179624808] There has been a previous report received where lack of water flow has caused an overheating insert. Since an overheating insert could necessitate medical/surgical intervention to preclude permanent damage to a body structure or permanent impairment of a body function, this malfunction would be likely to cause/contribute to a serious injury should it recur. As such, this event meets the criteria for reportability per 21 cfr part 803. Water tubing in hp cable restricted, possible reason for the overheating. No sterimate handpiece was sent in, could be the reason for overheating. Added new cable along with new water filter and foot pedal batteries.
Patient Sequence No: 1, Text Type: N, H10


[179624809] While using a g136 scaler, there was blocked water flow and the handpiece and water was getting hot; no injury resulted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2424472-2020-00002
MDR Report Key9682101
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-07
Date of Report2020-02-07
Date Mfgr Received2020-01-08
Date Added to Maude2020-02-07
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 Phone7178494229
Manufacturer G1DENTSPLY LLC
Manufacturer Street1301 SMILE WAY
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal Code17404
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCAVITRON PLUS PACKAGE
Generic NameSCALER, ULTRASONIC
Product CodeELC
Date Received2020-02-07
Returned To Mfg2020-01-15
Model NumberG136
Catalog Number8161425
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDENTSPLY LLC
Manufacturer Address1301 SMILE WAY YORK PA 17404 US 17404


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-07

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