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AFFECTED DEVICES

Philips Respironics is deploying a permanent corrective action to address the
two (2) issues described in the Field Safety Notification.* Please see the list
of affected devices and initiate the registration process below.


For more information on this Field Safety Notification*, please visit
Philips.com/SRC-Update


URGENT: FIELD SAFETY NOTIFICATION*




IF YOU ARE A PHYSICIAN, PLEASE CLICK HERE FOR MORE INFORMATION. IF YOU ARE A
PATIENT, DEVICE USER, CAREGIVER, DME, DISTRIBUTOR, PHARMACY, OR INSTITUTION,
BEGIN YOUR REGISTRATION BELOW:

This is a list of products affected globally. For a list of products affected in
your country please click here


ITEMS MARKED WITH AN ASTERISK (*) ARE REQUIRED.

CanadaUnited States of America (and
Territories)AlbaniaAlgeriaAndorraArgentinaAustraliaAustriaBahamasBahrainBangladeshBarbadosBelarusBelgiumBeninBermudaBoliviaBosnia
and HerzegovinaBrazilBruneiBulgariaCambodiaCameroonCayman
IslandsChileColombiaCosta RicaCroatiaCuraçaoCyprusCzech RepublicDenmarkDominican
RepublicEcuadorEgyptEl SalvadorEstoniaFinlandFranceFrench GuianaFrench
PolynesiaGeorgiaGermanyGhanaGreeceGuadeloupeGuatemalaHong
KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsraelItalyIvory Coast (Côte
d'Ivoire)JamaicaJapanJordanKenyaKosovoKuwaitLaosLatviaLebanonLibyaLithuaniaMalawiMalaysiaMaldivesMaltaMartiniqueMauritiusMayotteMexicoMonacoMontenegroMoroccoMyanmarNamibiaNepalNetherlandsNew
CaledoniaNew ZealandNigerNorth
MacedoniaNorwayOmanPakistanPanamaParaguayPeruPhilippinesPolandPortugalQatarReunionRomaniaSaint
Pierre and MiquelonSan MarinoSaudi
ArabiaSenegalSerbiaSingaporeSlovakiaSloveniaSouth AfricaSouth KoreaSpainSri
LankaSurinameSwedenSwitzerlandTaiwan (officially Republic of
China)TanzaniaThailandTrinidad and TobagoTunisiaTurkeyUkraineUnited Arab
EmiratesUnited KingdomUruguayUzbekistanVenezuelaVietnamYemenZimbabwe



* HIGHLIGHTED FIELD(S) IS/ARE REQUIRED.

Next

DME/Distributor/Pharmacy/Institution

Patient/Device User/Caregiver


I AM A: *


CHOOSE YOUR COUNTRY: *

BASED ON YOUR COUNTRY SELECTION, YOUR DME/DISTRIBUTOR/PHARMACY/INSTITUTION IS
RESPONSIBLE FOR MANAGING THE RECALL ON YOUR BEHALF.

* In Australia this is an Urgent Product Defect Correction and in New Zealand
this is a Recall for Product Correction



© 2024 : Philips

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