HUDSON DUAL HEATED DUAL DRAIN 880-36KIT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-02-07 for HUDSON DUAL HEATED DUAL DRAIN 880-36KIT manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number3004365956-2020-00033
MDR Report Key9681711
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-02-07
Date of Report2020-01-21
Date of Event2020-01-21
Date Mfgr Received2020-03-09
Date Added to Maude2020-02-07
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 ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUDSON DUAL HEATED DUAL DRAIN
Generic NameHUMIDIFIER NEBULIZER KIT
Product CodeOGG
Date Received2020-02-07
Returned To Mfg2019-01-29
Catalog Number880-36KIT
Lot Number74K1900013
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.