SMITHS MEDICAL BLUE LINE ULTRA TRACHEOSTOMY KIT 100/800/075CZ

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 2019-04-24 for SMITHS MEDICAL BLUE LINE ULTRA TRACHEOSTOMY KIT 100/800/075CZ manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[142934477] Information was received that while a patient under local anesthesia for cerebral infarction, was using a smiths medical tracheal tube kit. It was reported that patient's wound was oozing and air leaks were noted in the balloon. The tube was replaced immediately.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2019-02251
MDR Report Key8545274
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-24
Date of Report2019-04-24
Date of Event2018-12-04
Date Mfgr Received2019-03-26
Date Added to Maude2019-04-24
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 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833310
Manufacturer G1SMITHS MEDICAL CZECH REPUBLIC A.S.
Manufacturer StreetOLOMOUCK? 306
Manufacturer CityHRANICE, MESTO 753 01
Manufacturer CountryEZ
Manufacturer Postal Code753 01
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMITHS MEDICAL BLUE LINE ULTRA TRACHEOSTOMY KIT
Generic NameTRACHEOSTOMY
Product CodeOGW
Date Received2019-04-24
Catalog Number100/800/075CZ
Lot Number3484641
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-04-24

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