HUDSON ISO-GARD HEPA,SMALL STRAIGHT 28062

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-24 for HUDSON ISO-GARD HEPA,SMALL STRAIGHT 28062 manufactured by Teleflex Medical.

Event Text Entries

[125147691] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[125147692] Customer complaint alleges "there was a failure of measure co2 on the respirator. As it show up there was a small particle on the flowsensor. " alleged event reported occurred during a patient use. (cont. ) no patient consequence was reported. Patient condition reported as fine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8040412-2018-00279
MDR Report Key7999749
Date Received2018-10-24
Date of Report2018-10-08
Date of Event2018-10-04
Date Mfgr Received2018-11-21
Date Added to Maude2018-10-24
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 ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetPO BOX 28, KAMUNTING INDUSTRIAL ESTATE
Manufacturer CityPERAK, WEST MALAYSIA 34600
Manufacturer CountryMY
Manufacturer Postal Code34600
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHUDSON ISO-GARD HEPA,SMALL STRAIGHT
Product CodeCAH
Date Received2018-10-24
Catalog Number28062
Lot NumberUNKNOWN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressPERAK, WEST MALAYSIA


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-24

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