Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7. Recalled by GE Medical Systems, LLC Due to The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Medical Systems, LLC directly.
Affected Products
LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
Quantity: 31 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Medical Systems, LLC
GE Medical Systems, LLC has 146 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report