GE Medical Systems, LLC is recalling 133 LOGIQ P9 and P10 series ultrasound systems running software version R4.5.7. The software may provide inaccurate measurements of liver fat (liver steatosis), which could lead to incorrect medical assessments. This recall affects LOGIQ P9 and P10 models used in healthcare facilities for patient diagnostics.
Inaccurate measurements of liver fat may lead healthcare providers to make inappropriate clinical decisions regarding a patient's care, such as misdiagnosing liver disease or choosing an incorrect treatment plan. No specific injuries have been reported.
Recall #: Z-0155-2026; Quantity: 65 units
Recall #: Z-0156-2026; Quantity: 31 units
Recall #: Z-0157-2026; Quantity: 37 units
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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
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