PORTEX? BLUE LINE ULTRA? TRACHEOSTOMY TUBE 100/813/070CZ

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2020-03-17 for PORTEX? BLUE LINE ULTRA? TRACHEOSTOMY TUBE 100/813/070CZ manufactured by Smiths Medical Asd; Inc..

Event Text Entries

[183871924] Information was received indicating that the inner cannula to a smiths medical portex? Blue line ultra? Tracheostomy tube was noted to be broken. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-02107
MDR Report Key9845352
Report SourceFOREIGN,USER FACILITY
Date Received2020-03-17
Date of Report2020-03-17
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 CZECH REPUBLIC A. S.
Manufacturer StreetOLOMOUCK? 306
Manufacturer CityHRANICE 1-MESTO,
Manufacturer CountryEZ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX? BLUE LINE ULTRA? TRACHEOSTOMY TUBE
Generic NameTUBE TRACHEOSTOMY AND TUBE CUFF
Product CodeJOH
Date Received2020-03-17
Returned To Mfg2020-02-21
Catalog Number100/813/070CZ
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD; INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS,, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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