RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026SIEMENS HEALTHCARE LIMITEDOfficial source

    SOMATOM Definition Edge recall in Canada: Software defect

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    In plain language

    This recall involves SOMATOM Definition Edge medical devices sold in Canada. It's being recalled because a software defect may cause workflow interruptions. Contact the manufacturer for additional information.

    What to do

    • Contact the manufacturer if you require additional information.

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    Affected products

    • SOMATOM DEFINITION AS - MAIN UNIT

      Model: 8098027

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM DEFINITION FLASH SYS - MAIN

      Model: 10430603

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM DEFINITION EDGE SYSTEM - CT SYSTEM

      Model: 10590000

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM FORCE

      Model: 10742326

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM DRIVE

      Model: 10431700

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM CONFIDENCE - SYSTEM

      Model: 10590100

      Lot: ALL WITH INITIAL RELEASE VB20

    • SOMATOM EDGE PLUS

      Model: 10267000

      Lot: ALL WITH INITIAL RELEASE VB20

    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 WITH INITIAL RELEASE VB20

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: 10267000, 10430603, 10431700, 10590000, 10590100, 10742326, 8098027

    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 SOMATOM Definition Edge medical devices sold in Canada. It's being recalled because a software defect may cause workflow interruptions. Contact the manufacturer for additional information.

    What should consumers do?

    Contact the manufacturer if you require 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?

    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 November 19, 2021.

    Is the SIEMENS HEALTHCARE LIMITED brand affected by this recall?

    Yes, SIEMENS HEALTHCARE LIMITED products are affected by this recall. This recall involves SOMATOM Definition Edge medical devices sold in Canada. It's being recalled because a software defect may cause workflow interruptions. Contact the manufacturer for additional information.