HUDSON AQUAPAK 728 SW,760 ML W/028 ADAPTOR 037-28

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 2020-02-18 for HUDSON AQUAPAK 728 SW,760 ML W/028 ADAPTOR 037-28 manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number1417411-2020-00007
MDR Report Key9723199
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-02-18
Date of Report2020-01-31
Date of Event2020-01-22
Date Mfgr Received2020-02-24
Device Manufacturer Date2019-09-06
Date Added to Maude2020-02-18
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 Street900 WEST UNIVERSITY DR.
Manufacturer CityARLINGTON HEIGHTS IL 60004
Manufacturer CountryUS
Manufacturer Postal Code60004
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUDSON AQUAPAK 728 SW,760 ML W/028 ADAPTOR
Generic NameHUMIDIFIER NEBULIZER KIT
Product CodeOGG
Date Received2020-02-18
Returned To Mfg2020-02-10
Catalog Number037-28
Lot Number19F110
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-18

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