PORTEX? BIVONA? ADULT TTS? TRACHEOSTOMY TUBE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-27 for PORTEX? BIVONA? ADULT TTS? TRACHEOSTOMY TUBE manufactured by Smiths Medical Asd; Inc..

Event Text Entries

[185481912] Information was received indicating that three days following placement of a smiths medical portex? Uniperc? Adjustable tracheostomy tube, the cuff was not maintaining cuff pressure. The patient was reported to be obese which was reported to make the tube change out difficult. Following removal, the leak was noted to be at the attachment site of the pilot balloon. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02382
MDR Report Key9892384
Report SourceUSER FACILITY
Date Received2020-03-27
Date of Report2020-03-27
Date Mfgr Received2020-02-27
Date Added to Maude2020-03-27
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 N
Manufacturer CityMINNEAPOLIS,, MN
Manufacturer CountryUS
Manufacturer Phone3833310
Manufacturer G1SMITHS MEDICAL ASD; INC.
Manufacturer Street6000 NATHAN LANE N
Manufacturer CityMINNEAPOLIS,, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX? BIVONA? ADULT TTS? TRACHEOSTOMY TUBE
Generic NameTUBE TRACHEOSTOMY AND TUBE CUFF
Product CodeJOH
Date Received2020-03-27
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD; INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS,, MN US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-27

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