RecallGuide.ca
    Medical devices••Updated Jan 3, 2026•Philips Respironics•Official source

    Philips Respironics recalls several models of CPAP and BiLevel PAP machines and mechanical ventilators

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    This recall involves several models of Philips Respironics CPAP and BiLevel PAP machines and mechanical ventilators sold in Canada. They are being recalled due to performance issues. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Register your device on the Philips recall website or call 1-877-907-7508.
    • Talk to your physician or medical device provider before stopping or changing how you use your product.
    • Contact your health care provider or durable medical equipment provider to initiate the remediation process.

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    Affected products

    • BIPAP A30 SYSTEM-VENTILATOR

      Model: 1076577, 1111147

    • BIPAP A30 SYSTEM-VENTILATOR & SYSTEM ONE A-SERIES HEATED HUMIDIFIER

      Model: 1076578, 1111148

    • BIPAP A40, CANADA

      Model: 1076579, 1111173

    • BIPAP A40, CANADA, CORE PACKAGE

      Model: 1111174

    • BIPAP AUTO BI-FLEX, WITH HUMIDIFIER, WITH SMARTCARD, CANADA

      Model: CA751HS, CA761HBT, CA761HS, CA761NTS, CA761TBT, CA761TS

    • BIPAP AUTO BI-FLEX, WITH SMARTCARD, CANADA

      Model: CA751S, CA761BT, CA761S

    • BIPAP AUTOSV ADVANCED SYSTEM ONE

      Model: CA951HS, CA951S, CA961HS, CA961NTS, CA961S, CA961TS, CA961XHS, CA961XS, CA961XTS

    • BIPAP AUTOSV ADVANCED/ENCORE SMARTCARD

      Model: 1044288

    • BIPAP AUTOSV ADVANCED/ENCORE SMARTCARD/HEATED HUMIDIFIER

      Model: 1044289

    • BIPAP AUTOSV WITH SMARTCARD INT

      Model: 1044114

    • BIPAP AUTOSV WITH SMARTCARD INT, CORE PKG

      Model: 1044235

    • BIPAP AVAPS CORE PACKAGE, NORTH AMERICA

      Model: 1029750

    • BIPAP AVAPS VENTILATORY SUPPORT SYSTEM-CANADA

      Model: CA1060486, CA1161X, CAX1130S12

    • BIPAP AVAPS VENTILATORY SUPPORT SYSTEM-CORE PKG, CANADA

      Model: CA1061419, CA1161XTS, CAX1130H12, CAX1130H12C, CAX1130H12W, CAX1130T12, CAX1130T12C

    • BIPAP AVAPS, C SERIES VENTILAROTY SUPPORT SYSTEM-CORE PKG, DOMESTIC

      Model: 1061418

    • BIPAP AVAPS, C SERIES VENTILATORY SUPPORT SYSTEM-DOMESTIC

      Model: 1060485

    • BIPAP PRO BI-FLEX, WITH HUMIDIFIER, WITH SMARTCARD, CANADA

      Model: CA651HS, CA661HBT, CA661HS, CA661NTS, CA661TBT, CA661TS

    • BIPAP PRO BI-FLEX, WITH SMARTCARD, CANADA

      Model: CA651S, CA661S

    • BIPAP ST, C SERIES VENTILATORY SUPPORT SYSTEM, CORE PKG, CANADA

      Model: CA1061423

    • BIPAP ST, C SERIES VENTILATORY SUPPORT SYSTEM-CANADA

      Model: CA1061421

    • BIPAP ST, C SERIES VENTILATORY SUPPORT SYSTEM-CORE PKG, DOMESTIC

      Model: 1061422

    • BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM WITH SMARTCARD

      Model: 1029756, CA1029756

    • BIPAP SYNCHRONY VENTILATORY SUPPORT SYSTEM WITH SMARTCARD-CORE PACK

      Model: CA1029759

    • DREAMSTATION BIPAP PRO

      Model: CAX600H12, CAX600H12C, CAX600H12W, CAX600S12, CAX600T12, CAX600T12C

    • DREAMSTATION AUTO BIPAP

      Model: CAX700H12, CAX700H12C, CAX700H12W, CAX700S12, CAX700T12, CAX700T12C, CAX700T12W

    • DREAMSTATION AUTO CPAP

      Model: CAX500H12, CAX500H12C, CAX500H12W, CAX500S12, CAX500T12, CAX500T12C, CAX500T12W

    • DREAMSTATION BIPAP AUTO SV W/HUMID/HEATED TUBE, CA

      Model: CAX900T12, CAX900T12C

    • DREAMSTATION BIPAP AUTOSV, CA

      Model: CAX900S12

    • DREAMSTATION BIPAP AUTOSV, W/HUMIDIFIER, CA

      Model: CAX900H12

    • DREAMSTATION CPAP

      Model: CAX200H12, CAX200S12C, CAX200T12

    • DREAMSTATION CPAP PRO

      Model: CAX400H12, CAX400H12C, CAX400H12W, CAX400S12, CAX400T12, CAX400T12C, CAX400T12W

    • DREAMSTATION EXPERT

      Model: CAX501H12, CAX501H12C, CAX501T12, CAX5O1T12C, CAX5O1T12W

    • DREAMSTATION GO AUTO CPAP

      Model: CAG500S12

    • DREAMSTATION GO AUTO CPAP WITH HUMIDIFIER, CANADA

      Model: CAG500H12

    • DREAMSTATION GO CPAP

      Model: CAG400S12

    • DREAMSTATION GO CPAP WITH HUMIDIFIER, CANADA

      Model: CAG400H12

    • OMNILAB ADVANCED, DOMESTIC

      Model: 1111122

    • OMNILAB ADVANCED, DOMESTIC CORE

      Model: 1111123, 1111124

    • REMSTAR AUTO WITH HUMIDIFIER, WITH SD CARD, A-FLEX, CANADA

      Model: CA551HS, CA561HBT, CA561HS, CA561NTBT, CA561NTS, CA561TBT, CA561TS

    • REMSTAR AUTO WITH SD CARD, A-FLEX, CANADA

      Model: CA551S, CA561BT, CA561S

    • REMSTAR PLUS WITH HUMIDIFIER, WITH SD CARD, C-FLEX, CANADA

      Model: CA251HS, CA261HS, CA261NTS, CA261TS

    • REMSTAR PLUS WITH SD CARD, C-FLEX, CANADA

      Model: CA251S, CA261S

    • REMSTAR PRO WITH HUMIDIFIER, WITH SD CARD, C-FLEX +, CANADA

      Model: CA451HS, CA461HBT, CA461HS, CA461NTBT, CA461NTS, CA461TBT, CA461TS

    • REMSTAR PRO WITH SD CARD, C-FLEX +, CANADA

      Model: CA451S, CA461BT, CA461S

    • REMSTAR, WITH SMARTCARD, CANADA

      Model: CA151S

    • REMSTAR, WITH HUMIDIFIER, WITH SMARTCARD, CANADA

      Model: CA151HS

    • TRILOGY 100 VENTILATOR, CANADA

      Model: CA1054096, CA1054096B, U1054260

    • TRILOGY 100 VENTILATOR-INTERNATIONAL

      Model: 1054096, U1054096

    • TRILOGY 200, CANADA

      Model: CA1032800, CA1032800B

    Why this matters

    Performance issues

    View official recall notice

    Do I have this product?

    This recall only applies to specific products. Follow the steps below to check.

    1. 1

      Check the product name

      Make sure your product name matches one of the affected products listed above.

    2. 2

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 1029750, 1029756, 1044114, 1044235, 1044288, 1044289, 1054096, 1060485, 1061418, 1061422, 1076577, 1076578, 1076579, 1111122, 1111123, 1111124, 1111147, 1111148, 1111173, 1111174, CA1029756, CA1029759, CA1032800, CA1032800B, CA1054096, CA1054096B, CA1060486, CA1061419, CA1061421, CA1061423, CA1161X, CA1161XTS, CA151HS, CA151S, CA251HS, CA251S, CA261HS, CA261NTS, CA261S, CA261TS, CA451HS, CA451S, CA461BT, CA461HBT, CA461HS, CA461NTBT, CA461NTS, CA461S, CA461TBT, CA461TS, CA551HS, CA551S, CA561BT, CA561HBT, CA561HS, CA561NTBT, CA561NTS, CA561S, CA561TBT, CA561TS, CA651HS, CA651S, CA661HBT, CA661HS, CA661NTS, CA661S, CA661TBT, CA661TS, CA751HS, CA751S, CA761BT, CA761HBT, CA761HS, CA761NTS, CA761S, CA761TBT, CA761TS, CA951HS, CA951S, CA961HS, CA961NTS, CA961S, CA961TS, CA961XHS, CA961XS, CA961XTS, CAG400H12, CAG400S12, CAG500H12, CAG500S12, CAX1130H12, CAX1130H12C, CAX1130H12W, CAX1130S12, CAX1130T12, CAX1130T12C, CAX200H12, CAX200S12C, CAX200T12, CAX400H12, CAX400H12C, CAX400H12W, CAX400S12, CAX400T12, CAX400T12C, CAX400T12W, CAX500H12, CAX500H12C, CAX500H12W, CAX500S12, CAX500T12, CAX500T12C, CAX500T12W, CAX501H12, CAX501H12C, CAX501T12, CAX5O1T12C, CAX5O1T12W, CAX600H12, CAX600H12C, CAX600H12W, CAX600S12, CAX600T12, CAX600T12C, CAX700H12, CAX700H12C, CAX700H12W, CAX700S12, CAX700T12, CAX700T12C, CAX700T12W, CAX900H12, CAX900S12, CAX900T12, CAX900T12C, U1054096, U1054260

    If your product matches one or more of the details above, it may be affected by this recall.

    If your product does not match these details, it is not affected by this recall.

    When in doubt, always check the official notice.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Performance issues

    What should consumers do?

    Stop using the product immediately. Register your device on the Philips recall website or call 1-877-907-7508. Talk to your physician or medical device provider before stopping or changing how you use your product. Contact your health care provider or durable medical equipment provider to initiate the remediation process.

    Where was the product sold?

    This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.

    Is there a health risk?

    Yes, there may be a health risk. Performance issues

    When was this product recalled?

    This product was recalled on July 5, 2024.

    Is the Philips Respironics brand affected by this recall?

    Yes, Philips Respironics products are affected by this recall. This recall involves several models of Philips Respironics CPAP and BiLevel PAP machines and mechanical ventilators sold in Canada. They are being recalled due to performance issues. Stop using the product and follow the return/repair steps in the official notice.

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