ADULT DUAL HEATED EVAQUA2 BREATHING CIRCUIT RT380

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-01-22 for ADULT DUAL HEATED EVAQUA2 BREATHING CIRCUIT RT380 manufactured by Fisher & Paykel Healthcare Ltd.

Event Text Entries

[182587207] (b)(4). The complaint rt380 adult evaqua2 breathing circuit is currently en route to fisher & paykel healthcare (f&p) in (b)(4) for evaluation. We will provide a follow up report upon completion of our investigation.
Patient Sequence No: 1, Text Type: N, H10


[182587208] A distributor on behalf of a healthcare facility in (b)(6) reported, via a fisher & paykel healthcare (f&p) field representative, that an rt380 adult dual-heated evaqua2 breathing circuit failed ventilator leak test before use. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611451-2020-00077
MDR Report Key9618535
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-01-22
Date of Report2019-12-27
Date of Event2019-12-25
Date Mfgr Received2020-02-27
Device Manufacturer Date2019-07-12
Date Added to Maude2020-01-22
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 GAMAROONI
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 NameADULT DUAL HEATED EVAQUA2 BREATHING CIRCUIT
Generic NameBZE
Product CodeBZE
Date Received2020-01-22
Returned To Mfg2020-02-03
Model NumberRT380
Catalog NumberRT380
Lot Number2100822612
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 2020-01-22

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