RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026AngiotouchOfficial source

    Angiotouch Hand Controller Kit recall in Canada: expired product

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    In plain language

    This recall involves the Angiotouch Hand Controller Kit sold in Canada. It's being recalled because some kits were distributed after their expiration date. Stop using the product and follow the return steps in the official notice.

    What to do

    • Stop using the product immediately.
    • Check the lot number 07516N.
    • Contact Acist Medical Systems Inc. for return instructions.

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    Affected products

    • Angiotouch Hand Controller Kit

      Model: 014644

      Lot: 07516N

      Date codes: Expiration Date: 2017-03-29

    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 date code

      Date codes are usually printed near the best-before date or on the packaging seam.

      Affected date codes: Expiration Date: 2017-03-29

    3. 3

      Check the lot number

      Lot numbers identify specific production batches.

      Affected lots: 07516N

    4. 4

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 014644

    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?

    This recall involves the Angiotouch Hand Controller Kit sold in Canada. It's being recalled because some kits were distributed after their expiration date. Stop using the product and follow the return steps in the official notice.

    What should consumers do?

    Stop using the product immediately. Check the lot number 07516N. Contact Acist Medical Systems Inc. for return 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?

    A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.

    When was this product recalled?

    This product was recalled on January 8, 2018.

    Is the Angiotouch brand affected by this recall?

    Yes, Angiotouch products are affected by this recall. This recall involves the Angiotouch Hand Controller Kit sold in Canada. It's being recalled because some kits were distributed after their expiration date. Stop using the product and follow the return steps in the official notice.