FLEXITRUNK INFANT NASAL TUBING BC190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-05-02 for FLEXITRUNK INFANT NASAL TUBING BC190 manufactured by Fisher & Paykel Healthcare Limited.

Event Text Entries

[144007031] (b)(4). The complaint bc190 flexitrunk infant nasal tubings is currently en route to fisher & paykel healthcare (f&p) for evaluation. We are in process to determine if f&p's product caused or contributed to the reported event. We will provide a follow up report upon completion of our investigation.
Patient Sequence No: 1, Text Type: N, H10


[144007032] A healthcare facility in (b)(6) reported that the one of a bc190 flexitrunk infant nasal tubings was broken. There was no patient consequence.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611451-2019-00436
MDR Report Key8576287
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-05-02
Date of Report2019-04-03
Date Mfgr Received2019-07-04
Device Manufacturer Date2018-09-10
Date Added to Maude2019-05-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHARMACIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. FARANAK GOMAROONI
Manufacturer Street173 TECHNOLOGY DR., SUITE 100 IRVINE
Manufacturer CityCA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9494534000
Manufacturer G1FISHER & PAYKEL HEALTHCARE LIMITED
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 NameFLEXITRUNK INFANT NASAL TUBING
Generic NameBZO
Product CodeBZO
Date Received2019-05-02
Model NumberBC190
Catalog NumberBC190
Lot Number2100579709
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerFISHER & PAYKEL HEALTHCARE LIMITED
Manufacturer Address15 MAURICE PAYKEL PLACE EAST TAMAKI AUCKLAND, 2013 NZ 2013


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-02

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