HUDSON AQUAPAK 340 SW,340 ML W/040 ADAPTOR,JAP 003-40J

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 2019-11-19 for HUDSON AQUAPAK 340 SW,340 ML W/040 ADAPTOR,JAP 003-40J manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number1417411-2019-00059
MDR Report Key9340684
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-19
Date of Report2019-10-29
Date of Event2019-10-26
Date Mfgr Received2019-10-29
Device Manufacturer Date2019-02-11
Date Added to Maude2019-11-19
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 ContactVICTORIA SANDLIN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
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 340 SW,340 ML W/040 ADAPTOR,JAP
Generic NameHUMIDIFIER NEBULIZER KIT
Product CodeOGG
Date Received2019-11-19
Catalog Number003-40J
Lot Number19B059
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-19

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