TEC 6 PLUS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2018-09-25 for TEC 6 PLUS manufactured by Datex-ohmeda, Inc..

Event Text Entries

[121711376] A ge healthcare service representative performed a checkout of the equipment and confirmed the reported complaint. The vaporizer was replaced. No report of patient involvement.
Patient Sequence No: 1, Text Type: N, H10


[121711377] The hospital reported that, during preoperative testing, output of the vaporizer was higher than expected. There was no report of patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2112667-2018-01885
MDR Report Key7906764
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2018-09-25
Date of Report2018-09-25
Date of Event2018-08-30
Date Mfgr Received2018-08-30
Device Manufacturer Date2012-07-26
Date Added to Maude2018-09-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJOHN SZALINSKI
Manufacturer Street3000 N GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTEC 6 PLUS
Generic NameVAPORIZER
Product CodeCAD
Date Received2018-09-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDATEX-OHMEDA, INC.
Manufacturer Address3030 OHMEDA DR, MADISON, WI 53718 US 53718


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-25

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