GE Medical recalls LOGIQ P10 ultrasound devices with software version R4.5.7 that may show inaccurate liver fat measurements, potentially leading to incorrect medical decisions.
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.
GE Medical is recalling LOGIQ P10 ultrasound devices with software version R4.5.7 because they might display incorrect liver fat measurements. This could lead to inappropriate medical decisions if doctors rely on the inaccurate data.
The device's Ultrasound-Guided Attenuation Parameter (UGAP) measurement may show incorrect liver fat levels. This could cause doctors to make treatment choices that aren't based on accurate information, potentially affecting patient care.
Healthcare providers using the LOGIQ P10 ultrasound devices with software version R4.5.7 are most at risk. Patients receiving care from these devices may be affected if the inaccurate liver fat readings influence treatment decisions.
Check for the model number 5877534 and software version R4.5.7 on the device. The serial numbers listed in the recall notice include LPX441358 and other specific numbers.
Look for the software version on the device's display or settings menu to confirm if it is R4.5.7.
The recall is happening because the Ultrasound-Guided Attenuation Parameter (UGAP) measurement may display inaccurate liver fat values, which could lead to inappropriate clinical decisions.
The recall does not specify a remedy, so no action is required unless you notice inaccurate liver fat measurements and consult your healthcare provider.
Check for the model number 5877534 and software version R4.5.7. The serial numbers listed in the recall include LPX441358 and other specific numbers.
We’ve drafted a message you can send GE Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0155-2026 — GE Medical GE Medical Hello, I own a GE Medical that is covered by recall Z-0155-2026 from GE Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
