PORTEX ADULT TTS ADJUSTABLE NECK FLANGE HYPERFLEX TRACHEOSTOMY TUBE 67HA70

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-03-29 for PORTEX ADULT TTS ADJUSTABLE NECK FLANGE HYPERFLEX TRACHEOSTOMY TUBE 67HA70 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[185481592] Information was received that a patient's portex adult tts adjustable neck flange hyperflex tracheostomy tube leaked. No adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02398
MDR Report Key9895013
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2020-03-29
Date of Report2020-03-28
Date of Event2020-02-24
Date Mfgr Received2020-02-27
Date Added to Maude2020-03-29
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 ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street5700 WEST 23RD AVENUE
Manufacturer CityGARY, IN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX ADULT TTS ADJUSTABLE NECK FLANGE HYPERFLEX TRACHEOSTOMY TUBE
Generic NameTUBE TRACHEOSTOMY AND TUBE CUFF, PRODUCT CODE: JOH
Product CodeJOH
Date Received2020-03-29
Returned To Mfg2020-03-25
Catalog Number67HA70
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-29

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