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    Medical devicesUpdated Jan 3, 2026BDOfficial source

    Medical devices recall in Canada: Fluid may escape

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    In plain language

    This recall involves several medical devices, including Administration Sets and Extension Sets, sold in Canada. They are being recalled because fluid may escape upon disconnection from the BD MaxZero connector. BD is updating instructions for use to address this issue. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model numbers if provided.
    • Follow the updated instructions for use from BD.

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    Affected products

    • Administration Set with 2 Connectors

      Model: MZ5313, MZ5316

      Lot: All lots

    • Administration Set with 1 Connector

      Model: MZ5312, MZ8002, MZ8003, MZT1003, MZT1004, MZX5301, MZX5302, MZXT5303, MZXT5307, MZXT9004

      Lot: All lots

    • Administration Set with 3 Connectors

      Model: MZ8001, MZ9313, MZXT9003

      Lot: All lots

    • Standard Bore Extension Set with Bonded MaxPlus Connector

      Model: MZ5303, MZ5304, MZ5305, MZ5308, MZ5309, MZ5310, MZ9280

      Lot: All lots

    • Minibore Extension Set

      Model: MZ5301, MZ5302, MZ5306, MZ5307, MZ9226, MZ9265, MZ9266, MZ9267, MZ9270, MZ9271, MZ9272, MZ9273, MZ9274, MZ9275, MZ9276, MZ9277, MZ9278, MZ9279, MZ9281, MZ9283, MZXT9001

      Lot: All lots

    • MaxPlus Positive Pressure Needleless IV Connector

      Model: MZ1000-07

      Lot: All lots

    Why this matters

    Fluid escape

    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 lot number

      Lot numbers identify specific production batches.

      Affected lots: All lots

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: MZ1000-07, MZ5301, MZ5302, MZ5303, MZ5304, MZ5305, MZ5306, MZ5307, MZ5308, MZ5309, MZ5310, MZ5312, MZ5313, MZ5316, MZ8001, MZ8002, MZ8003, MZ9226, MZ9265, MZ9266, MZ9267, MZ9270, MZ9271, MZ9272, MZ9273, MZ9274, MZ9275, MZ9276, MZ9277, MZ9278, MZ9279, MZ9280, MZ9281, MZ9283, MZ9313, MZT1003, MZT1004, MZX5301, MZX5302, MZXT5303, MZXT5307, MZXT9001, MZXT9003, MZXT9004

    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?

    Fluid escape

    What should consumers do?

    Stop using the product immediately. Check model numbers if provided. Follow the updated instructions for use from BD.

    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. Fluid escape

    When was this product recalled?

    This product was recalled on May 10, 2019.

    Is the BD brand affected by this recall?

    Yes, BD products are affected by this recall. This recall involves several medical devices, including Administration Sets and Extension Sets, sold in Canada. They are being recalled because fluid may escape upon disconnection from the BD MaxZero connector. BD is updating instructions for use to address this issue. Stop using the product and follow the return/repair steps in the official notice.