RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026RiftonOfficial source

    Rifton TRAM and E-Pacer recall in Canada: Fall risk

    Share:

    In plain language

    This recall involves Rifton TRAM and E-Pacer medical devices sold in Canada. They are being recalled because a strap defect could cause a user to fall. Stop using the product and follow the return/repair steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Contact Rifton to receive a body support upgrade kit.
    • Install the upgrade kit as instructed.

    Get alerts for recalls like this

    Get email alerts when new recalls affect products in this category.

    Categories (optional)

    No spam. Unsubscribe anytime. We only email when there's a relevant recall.

    Affected products

    • TRAM

      Model: K310, K320

      Lot: More than 10 numbers, contact manufacturer.

    • E-Pacer

      Model: K660

      Lot: More than 10 numbers, contact manufacturer.

    Why this matters

    Fall risk for the user

    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: More than 10 numbers, contact manufacturer.

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: K310, K320, K660

    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.

    Want alerts if similar products are recalled in Canada?

    Frequently Asked Questions

    Why was this product recalled?

    Fall risk for the user

    What should consumers do?

    Stop using the product immediately. Contact Rifton to receive a body support upgrade kit. Install the upgrade kit as instructed.

    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. Fall risk for the user

    When was this product recalled?

    This product was recalled on December 17, 2025.

    Is the Rifton brand affected by this recall?

    Yes, Rifton products are affected by this recall. This recall involves Rifton TRAM and E-Pacer medical devices sold in Canada. They are being recalled because a strap defect could cause a user to fall. Stop using the product and follow the return/repair steps in the official notice.