GE Medical Systems, LLC recalls LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7., Model Number 5877533
- Recall date
- September 18, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0157-2026
- FDA classification
- Class II
- Brand / firm
- GE Medical Systems, LLC
- Sold / distributed
- US Nationwide. Global Distribution.
Why it was 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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7., Model Number 5877533
Get recall alerts
Free email alert whenever GE Medical Systems, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: GE Medical Systems, LLC