RecallGuide.ca
    Medical devicesUpdated Jan 3, 2026GEOfficial source

    Optima NM/CT 640 Unit, Discovery NM/CT (670 CZT, 670 ES), Discovery 670 DR, NM/CT (870 DR, 870 CZT), NM 830 (2019-03-19)

    Share:

    In plain language

    This recall involves several GE nuclear medicine systems, including Optima NM/CT 640 Unit and Discovery NM/CT models, used in healthcare settings in Canada. They are being recalled because some detector screws may not have been secured correctly during installation, which could lead to the detector falling and causing bodily harm. Healthcare professionals should follow the instructions in the official notice.

    What to do

    • Stop using the affected medical devices.
    • Check the model and serial numbers of your units.
    • Follow the instructions from GE Medical Systems Israel for inspection and repair.

    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

    • Optima NM/CT 640 Unit

      Model: H3100YD

      Lot: ONMX26480, ONMX26502

    • Discovery NM/CT 670 CZT

      Model: H3906CU

      Lot: AD7X38019

    • Discovery NM/CT 670 ES

      Model: H3100BK

      Lot: ESDX35020

    • Discovery 670 DR

      Model: H3100AL

      Lot: DRGX56004

    • NM/CT 870 DR

      Model: H3100AR

      Lot: 870Y64034

    • NM/CT 870 CZT

      Model: H3906CV

      Lot: 87CX63015

    • NM 830

      Model: H3910AB

      Lot: 830X60022

    Why this matters

    Bodily harm from falling detector

    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: 830X60022, 870Y64034, 87CX63015, AD7X38019, DRGX56004, ESDX35020, ONMX26480, ONMX26502

    3. 3

      Check the model number

      Model numbers are typically on the product label or packaging.

      Affected models: H3100AL, H3100AR, H3100BK, H3100YD, H3906CU, H3906CV, H3910AB

    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?

    Bodily harm from falling detector

    What should consumers do?

    Stop using the affected medical devices. Check the model and serial numbers of your units. Follow the instructions from GE Medical Systems Israel for inspection and repair.

    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. Bodily harm from falling detector

    When was this product recalled?

    This product was recalled on April 12, 2019.

    Is the GE brand affected by this recall?

    Yes, GE products are affected by this recall. This recall involves several GE nuclear medicine systems, including Optima NM/CT 640 Unit and Discovery NM/CT models, used in healthcare settings in Canada. They are being recalled because some detector screws may not have been secured correctly during installation, which could lead to the detector falling and causing bodily harm. Healthcare professionals should follow the instructions in the official notice.