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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

GE Healthcare, LLC: 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 a

Agency Publication Date: May 11, 2021
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Affected Products

Product: NM/CT 850 Nuclear Medicine / CT Scanners

GTIN*00840682140775

Product: NM/CT 860 Nuclear Medicine / CT Scanners

GTIN*00840682140751

Product: NM/CT 870 DR Nuclear Medicine / CT Scanners

GTIN*00840682140836

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87811
Status: Active
Manufacturer: GE Healthcare, LLC
Manufactured In: United States
Units Affected: 3 products (242 in total (17 units US))
Agency Last Updated: November 9, 2021

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.