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NMCTRecalls & reported problems across all models

G E Medical Systems Israel Ltd. · 3 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

4 open recalls name at least one NMCT model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
4

We found 3 models of NMCT by G E Medical Systems Israel Ltd. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

4 FDA recall records name at least one of these models by its device identifier, 4 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

NMCT recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Dec 19, 2022Class IOpen, Classified

    A mitigation may not be correctly implemented. If this is the case, the detector can fall, leading to life-threatening bodily injury.

    Z-1058-2023 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

  2. Feb 7, 2021Class IIOpen, Classified

    GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

    Z-1547-2021 · Root cause: Device Design · Recall details · FDA record ↗

  3. Feb 7, 2021Class IIOpen, Classified

    GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

    Z-1546-2021 · Root cause: Device Design · Recall details · FDA record ↗

  4. Feb 7, 2021Class IIOpen, Classified

    GE Healthcare has become aware of a potential issue on 800 family NM/CT Scanners that could cause a shift in CT radiation exposure range of up to 5cm compared to the intended radiation exposure range of the planned scan under specific workflows. The issue occurs only on a hybrid whole-body continuous F3 protocol with Zoom < 1 where the scan range is set on the Smart Console. In some cases, this may also necessitate a re-scan of the patient, which would expose the patient to additional X-ray radiation.

    Z-1545-2021 · Root cause: Device Design · Recall details · FDA record ↗

NMCT models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other G E Medical Systems Israel Ltd. products

All G E Medical Systems Israel Ltd. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page