PORTEX THORACIC CATHETER SELDINGER CHEST DRAINAGE KIT 200/910/120

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 2019-11-07 for PORTEX THORACIC CATHETER SELDINGER CHEST DRAINAGE KIT 200/910/120 manufactured by Smiths Medical Asd, Inc..

MAUDE Entry Details

Report Number3012307300-2019-05948
MDR Report Key9292547
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-07
Date of Report2019-11-07
Date of Event2019-10-10
Date Mfgr Received2019-10-11
Device Manufacturer Date2019-07-17
Date Added to Maude2019-11-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 G1SMITHS MEDICAL INTERNATIONAL LTD.
Manufacturer StreetBOUNDARY ROAD, HYTHE KENT CT21 6JL
Manufacturer CityKENT,
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTEX THORACIC CATHETER SELDINGER CHEST DRAINAGE KIT
Generic NameCHEST DRAINAGE KIT
Product CodePAD
Date Received2019-11-07
Returned To Mfg2019-10-21
Model Number200/910/120
Catalog Number200/910/120
Lot Number3832304
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
101. Life Threatening; 2. Required No Informationntervention 2019-11-07

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