PORTEX? ENDOBRONCHIAL TUBE 198-35L

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-01-03 for PORTEX? ENDOBRONCHIAL TUBE 198-35L manufactured by Smiths Medical Asd; Inc..

Event Text Entries

[175848817] Information was received indicating that the slip joint to a smiths medical portex? Endobronchial tube became detached from the y-site connector. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-00489
MDR Report Key9549556
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-03
Date of Report2020-02-19
Date Mfgr Received2020-01-21
Date Added to Maude2020-01-03
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 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833310
Manufacturer G1SMITHS MEDICAL INTERNATIONAL LTD.
Manufacturer StreetBOUNDARY ROAD
Manufacturer CityHYTHE, CT216JL
Manufacturer CountryUK
Manufacturer Postal CodeCT21 6JL
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX? ENDOBRONCHIAL TUBE
Generic NameTUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)
Product CodeCBI
Date Received2020-01-03
Returned To Mfg2020-01-03
Model Number198-35L
Catalog Number198-35L
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD; INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS, MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-03

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