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

    QUANTA-Lyser 3000 recall in Canada: communication interruption

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    In plain language

    This recall involves the QUANTA-Lyser 3000 medical device sold in Canada. It's being recalled because a cable dongle may interrupt communication during testing. This requires operators to restart testing and can lead to no test results being generated.

    What to do

    • Stop using the product immediately.
    • Check model numbers if provided.
    • Follow the return/repair steps in the official notice.

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    Affected products

    • QUANTA-Lyser 3000

      Model: 066VS3000

    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: 066VS3000

    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.

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    Frequently Asked Questions

    Why was this product recalled?

    This recall involves the QUANTA-Lyser 3000 medical device sold in Canada. It's being recalled because a cable dongle may interrupt communication during testing. This requires operators to restart testing and can lead to no test results being generated.

    What should consumers do?

    Stop using the product immediately. Check model numbers if provided. Follow the return/repair steps in the official notice.

    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 June 14, 2019.