CUSTOMIZED PORTEX BIVONA TRACHEOSTOMY TUBE ST17FN70NSB128N

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-03-21 for CUSTOMIZED PORTEX BIVONA TRACHEOSTOMY TUBE ST17FN70NSB128N manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[184422424] Possible lot number are: bs001477, bs002617, bs002618.
Patient Sequence No: 1, Text Type: N, H10


[184422425] Information was received that a smiths medical customized portex bivona tracheostomy tube, had issues, pinching the patient. No further adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02118
MDR Report Key9863269
Report SourceDISTRIBUTOR
Date Received2020-03-21
Date of Report2020-03-20
Date Mfgr Received2020-02-19
Device Manufacturer Date2019-07-11
Date Added to Maude2020-03-21
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 NameCUSTOMIZED PORTEX BIVONA TRACHEOSTOMY TUBE
Generic NameTUBTUBE, TRACHEOSTOMY (W/WO CONNECTOR) PRODUCT CODE: BTO
Product CodeBTO
Date Received2020-03-21
Model NumberST17FN70NSB128N
Catalog NumberST17FN70NSB128N
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-21

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