RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026Official source

    Therapy Chair Coil Arm recall in Canada: arm may fail during use

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    In plain language

    This recall involves Therapy Chair Coil Arms sold in Canada. It's being recalled because the coil arm may fail during use, or become loose or disconnected. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check model number 280111.
    • Contact The Magstim Company Limited for instructions.

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    Affected products

    • Therapy Chair Coil Arm

      Model: 280111

      Lot: All Lots

    Why this matters

    Injury risk from product failure

    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: 280111

    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?

    Injury risk from product failure

    What should consumers do?

    Stop using the product immediately. Check model number 280111. Contact The Magstim Company Limited for 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?

    Yes, there may be a health risk. Injury risk from product failure

    When was this product recalled?

    This product was recalled on February 15, 2019.