GE Medical Systems recalls LOGIQ P10 R4.5 HD ultrasound systems with software version R4.5.7. Model 5877535 may display inaccurate liver fat measurements, risking wrong 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 Systems is recalling certain LOGIQ P10 R4.5 HD ultrasound systems with software version R4.5.7. These units may show inaccurate liver fat measurements, which could lead to incorrect medical treatments.
The ultrasound system's UGAP measurement feature may display inaccurate values for liver steatosis. This could cause doctors to make wrong treatment choices based on faulty data.
Healthcare providers using the recalled ultrasound systems with model number 5877535 and software version R4.5.7 are most at risk of receiving incorrect liver fat assessments.
Check for model number 5877535 and software version R4.5.7 on the device. The serial numbers listed in the recall notice include LPZ490338 and other specific numbers.
Verify the software version on your LOGIQ P10 R4.5 HD ultrasound system to see if it is R4.5.7.
This recall affects LOGIQ P10 R4.5 HD ultrasound systems with model number 5877535 and software version R4.5.7. Check your device details to see if you are affected.
The recall does not specify a remedy, so no action is required unless you are concerned about inaccurate liver fat measurements. Contact GE Medical Systems for further assistance.
The recall states that inaccurate measurements could lead to inappropriate clinical decisions, but it does not mention a risk of serious injury. This is a low-risk issue.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0156-2026 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0156-2026 from GE Healthcare. 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.
