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    Medical devicesUpdated Jan 3, 2026AirLifeOfficial source

    AirLife ABG Samplers recall in Canada: labeling error

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    In plain language

    This recall involves AirLife Arterial Blood Gas (ABG) Sampling Aspirators, Micro and Quick AGB Samplers sold in Canada. They are being recalled because of an error in labeling where "luer slip" was incorrectly printed instead of "luer lock" on the product description. Stop using the product and follow the return steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for return instructions.

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    Affected products

    Specific affected products are listed in the official notice.

    Do I have this product?

    This recall applies to specific products. Details are listed in the official notice.

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    Frequently Asked Questions

    Why was this product recalled?

    This recall involves AirLife Arterial Blood Gas (ABG) Sampling Aspirators, Micro and Quick AGB Samplers sold in Canada. They are being recalled because of an error in labeling where "luer slip" was incorrectly printed instead of "luer lock" on the product description. Stop using the product and follow the return steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Contact the manufacturer for return instructions.

    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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on October 5, 2018.

    Is the AirLife brand affected by this recall?

    Yes, AirLife products are affected by this recall. This recall involves AirLife Arterial Blood Gas (ABG) Sampling Aspirators, Micro and Quick AGB Samplers sold in Canada. They are being recalled because of an error in labeling where "luer slip" was incorrectly printed instead of "luer lock" on the product description. Stop using the product and follow the return steps in the official notice.