Medical devicesUpdated Jan 3, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Official source

    Ingenia 3.0T recall in Canada: Performance issue

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    In plain language

    This recall involves the Philips Ingenia 3.0T MR system, a medical device sold in Canada. It's being recalled because screws in the patient support may come loose, potentially blocking movement of the tabletop. This recall is for healthcare facilities.

    What to do

    • Contact the manufacturer for additional information.

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    Affected products

    • Ingenia 3.0T

      Model: 782103

      Lot: 34055

    Why this matters

    Performance issue with medical device

    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: 34055

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 782103

    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?

    Performance issue with medical device

    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. Performance issue with medical device

    When was this product recalled?

    This product was recalled on September 13, 2024.

    Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. brand affected by this recall?

    Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. products are affected by this recall. This recall involves the Philips Ingenia 3.0T MR system, a medical device sold in Canada. It's being recalled because screws in the patient support may come loose, potentially blocking movement of the tabletop. This recall is for healthcare facilities.