GE Medical recalls LOGIQ P9 R4.5 ultrasound systems with software version R4.5.7 (model 5877533) due to potential inaccurate liver steatosis measurements, which could lead to inappropriate clinical 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 specific models of LOGIQ P9 R4.5 ultrasound systems with software version R4.5.7. This recall is because the device may display inaccurate liver fat measurements, which could lead to incorrect medical decisions.
The ultrasound system's UGAP (Ultrasound-Guided Attenuation Parameter) measurement may show inaccurate values for liver steatosis. This could cause doctors to make wrong treatment choices based on the faulty data.
Healthcare providers using the recalled ultrasound systems with model number 5877533 and software version R4.5.7 are most at risk of receiving incorrect liver fat measurements.
Check if your LOGIQ P9 R4.5 ultrasound system has software version R4.5.7 and model number 5877533. The serial numbers listed in the recall include LP9490416 and other specific numbers.
Verify your ultrasound system's software version is R4.5.7 and model number 5877533.
The ultrasound system may display inaccurate liver fat measurements, which could lead to inappropriate clinical decisions.
Check if your system has software version R4.5.7 and model number 5877533. If so, contact GE Medical for further instructions.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send GE Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0157-2026 — GE Medical GE Medical Hello, I own a GE Medical that is covered by recall Z-0157-2026 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.
