HEATED BREATHING TUBE 900PT561

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 2020-01-16 for HEATED BREATHING TUBE 900PT561 manufactured by Fisher & Paykel Healthcare Ltd.

Event Text Entries

[182569105] (b)(4). We are in the process of obtaining the complaint device for investigation. We will provide a follow up report upon completion of our investigation.
Patient Sequence No: 1, Text Type: N, H10


[182569106] A hospital in (b)(6) reported via a fisher & paykel (f&p) representative that a 900pt561 airvo heated breathing tube used with an airvo2 humidifier was covered under a pillow. The circuit was found melted. This was found during use. No patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611451-2020-00063
MDR Report Key9594732
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-01-16
Date of Report2019-12-17
Date of Event2019-12-13
Date Mfgr Received2020-02-24
Date Added to Maude2020-01-16
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 ContactMS FARANAK GOMAROONI
Manufacturer Street173 TECHNOLOGY DRIVE SUITE 100
Manufacturer CityIRVINE, CA CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9494534000
Manufacturer G1FISHER & PAYKEL HEALTHCARE LTD
Manufacturer Street15 MAURICE PAYKEL PLACE EAST TAMAKI
Manufacturer CityAUCKLAND, 2013
Manufacturer CountryNZ
Manufacturer Postal Code2013
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHEATED BREATHING TUBE
Generic NameAIRVO HEATED BREATHING TUBE
Product CodeBZE
Date Received2020-01-16
Returned To Mfg2020-02-03
Model Number900PT561
Catalog Number900PT561
Lot NumberNOT PROVIDED
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerFISHER & PAYKEL HEALTHCARE LTD
Manufacturer Address15 MAURICE PAYKEL PLACE EAST TAMAKI AUCKLAND, 2013 NZ 2013


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-16

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