TEC 6 PLUS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2015-12-22 for TEC 6 PLUS manufactured by Datex-ohmeda, Inc..

Event Text Entries

[34128424] The unit was returned to ge healthcare for investigation. The unit was inspected and it was noted that the interlock plunger pin circlip was missing. The part was replaced and the unit is operational.
Patient Sequence No: 1, Text Type: N, H10


[34128425] During routine installation testing, the ge healthcare service representative noted the interlock system was not functional. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2112667-2015-00441
MDR Report Key5317745
Report SourceCOMPANY REPRESENTATIVE
Date Received2015-12-22
Date of Report2015-12-08
Date of Event2015-12-08
Date Mfgr Received2015-12-08
Device Manufacturer Date2014-08-12
Date Added to Maude2015-12-22
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 FDA3
Event Location3
Manufacturer ContactSTEPHANIE CASS
Manufacturer Street3000 N. GRANDVIEW BOULEVARD
Manufacturer CityWAUKESHA WI 531881696
Manufacturer CountryUS
Manufacturer Postal531881696
Manufacturer G1DATEX-OHMEDA, INC.
Manufacturer Street3030 OHMEDA DRIVE
Manufacturer CityMADISON WI 53718
Manufacturer CountryUS
Manufacturer Postal Code53718
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTEC 6 PLUS
Generic NameVAPORIZER
Product CodeCAD
Date Received2015-12-22
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDATEX-OHMEDA, INC.
Manufacturer Address3030 OHMEDA DRIVE MADISON WI 53718 US 53718


Patients

Patient NumberTreatmentOutcomeDate
10 2015-12-22

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