Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0156-2026 — LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535

U.S. FDA — Device Enforcement · United States · 2025-09-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0156-2026
Date of alert
2025-09-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Medical Systems, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00195278464668
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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