PORTEX BIVONA FLEXTEND? TTS? TRACHEOSTOMY TUBE 67PFSS50

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-03-17 for PORTEX BIVONA FLEXTEND? TTS? TRACHEOSTOMY TUBE 67PFSS50 manufactured by Smiths Medical Asd; Inc..

Event Text Entries

[183875080] Three complaint files are related to each other. However, only two files are found reportable. Cc-0067641 was found not reportable as fault was found at pre-use check. 3012307300-2020-02099-0067642 is the third complaint in the series.
Patient Sequence No: 1, Text Type: N, H10


[183875081] Information was received indicating that immediately following placement of a smiths medical portex bivona flextend? Tts? Tracheostomy tube the patient desaturated and turned blue. The patient was then bagged while the trach tube was removed, and the cuff massaged. The cuff was re-inflated but was reported to only inflate to 30-40%. A second cuff was attempted to be used but once again, cuff would not inflate fully. Subsequently, one of the patient's old tracheostomy tubes was used but was reported to have mold inside the cuff. The patient recovered but is currently awaiting further replacement trach tubes.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02112
MDR Report Key9845355
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2020-02-09
Date Mfgr Received2020-02-19
Date Added to Maude2020-03-17
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 FLEXTEND? TTS? TRACHEOSTOMY TUBE
Generic NameTUBE TRACHEOSTOMY AND TUBE CUFF
Product CodeJOH
Date Received2020-03-17
Model Number67PFSS50
Catalog Number67PFSS50
OperatorLAY USER/PATIENT
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. Life Threatening; 2. Required No Informationntervention 2020-03-17

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