RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Technomed EuropeOfficial source

    Disposable Subdermal EEG Needle Electrode recall in Canada: mechanical defect

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    In plain language

    This recall involves Disposable Subdermal EEG Needle Electrodes sold in Canada. They are being recalled due to a mechanical defect where the needle may dislodge. Stop using the product and contact the manufacturer for more information.

    What to do

    • Stop using the product immediately.
    • Contact the manufacturer for additional information.

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    Affected products

    • Disposable Subdermal Eeg Needle Electrode

      Model: TE/S50715-001

      Lot: 49192, 49429, 50106

    Why this matters

    Mechanical defect

    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: 49192, 49429, 50106

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: TE/S50715-001

    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?

    Mechanical defect

    What should consumers do?

    Stop using the product immediately. 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. Mechanical defect

    When was this product recalled?

    This product was recalled on January 4, 2022.

    Is the Technomed Europe brand affected by this recall?

    Yes, Technomed Europe products are affected by this recall. This recall involves Disposable Subdermal EEG Needle Electrodes sold in Canada. They are being recalled due to a mechanical defect where the needle may dislodge. Stop using the product and contact the manufacturer for more information.