GE Healthcare recalls LOGIQ F R3 ultrasound systems with model 5943263 due to potential incorrect fetal weight calculations affecting clinical decisions. Learn about affected units and safety steps.
GE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previous obstetric patient data in the Whizz report. This could potentially lead to an incorrect clinical decision due to inaccuracy in the fetal size and growth calculation.
GE Healthcare is recalling specific models of their LOGIQ F R3 ultrasound systems because the Estimated Fetal Weight feature may display outdated patient data, leading to inaccurate fetal size calculations. This could cause incorrect clinical decisions during pregnancy monitoring if not addressed.
The ultrasound system's Estimated Fetal Weight feature can show previous obstetric patient data in the Whizz report. This might cause the system to calculate fetal size and growth incorrectly, potentially leading to wrong clinical decisions about pregnancy health.
Pregnant patients using the recalled LOGIQ F R3 ultrasound systems with model number 5943263 are at risk of receiving incorrect fetal weight measurements. Healthcare providers using these systems for prenatal care may need to adjust their clinical decisions.
Check for the model number 5943263 on the ultrasound system. Affected units have specific serial numbers listed in the recall notice, including 6310028WX0 through 6310043WX0.
Verify the model number on your GE Healthcare LOGIQ F R3 ultrasound system to see if it matches 5943263.
Check if your system's serial number is among the listed numbers: 6310028WX0, 6310008WX0, 6310041WX0, and other specific serial numbers provided in the recall.
The recall is because the Estimated Fetal Weight feature may display previous obstetric patient data, which could lead to inaccurate fetal size calculations and incorrect clinical decisions.
Check if your model number is 5943263 and if your serial number is listed in the recall notice. If affected, contact GE Healthcare for guidance.
This is a low-risk issue as it involves potential incorrect measurements, not physical harm. The hazard does not cause immediate injury or death.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2029-2025 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2029-2025 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.