RecallGuide.ca
    Medical devicesUpdated Jan 6, 2026Jumper MedicalOfficial source

    Jumper Medical Fetal Doppler

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    In plain language

    This recall involves Jumper Medical Fetal Dopplers sold in Canada. It's being recalled because using these devices at home without professional supervision may pose risks. Health Canada is revising product labels to remove claims of home use.

    What to do

    • Contact the manufacturer for additional information.

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    Affected products

    • Fetal Doppler

      Model: JPD-100B, JPD-100E, JPD-100S, JPD-100S6, JPD-100SMINI

    Why this matters

    Risks from unsupervised home use

    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: JPD-100B, JPD-100E, JPD-100S, JPD-100S6, JPD-100SMINI

    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?

    Risks from unsupervised home use

    What should consumers do?

    Contact the manufacturer for additional information.

    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. Risks from unsupervised home use

    When was this product recalled?

    This product was recalled on January 6, 2026.

    Is the Jumper Medical brand affected by this recall?

    Yes, Jumper Medical products are affected by this recall. This recall involves Jumper Medical Fetal Dopplers sold in Canada. It's being recalled because using these devices at home without professional supervision may pose risks. Health Canada is revising product labels to remove claims of home use.