RecallRadar

FDA Device recall Z-0156-2026

LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535

On 2025-10-22 the FDA classified a Class II recall of LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535 by Ge Medical Systems, citing the Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinic….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0156-2026
ClassificationClass II
Statusongoing
Initiated2025-09-18
Published2025-10-22
Last updated2026-09-13 11:57 UTC
CompanyGe Medical Systems
DistributionUS

Product

LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535

Reason

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.

Identifiers

code_info
Model Number 5877535 UDI-DI: 00195278464668, Serial Numbers: LPZ490338 LPZ490347 LPZ490339 LPZ490147 LPZ490292 LPZ49001…Model Number 5877535 UDI-DI: 00195278464668, Serial Numbers: LPZ490338 LPZ490347 LPZ490339 LPZ490147 LPZ490292 LPZ490019 LPZ490252 LPZ490348 LPZ490303 LPZ490304 LPZ490305 LPZ490306 LPZ490340 LPZ490350 LPZ490341 LPZ440658 LPZ440673 LPZ440674 LPZ490337 LPZ440641 LPZ440192 LPZ440258 LPZ440694 LPZ440695 LPZ440692 LPZ440632 LPZ440185 LPZ440107 LPZ440168 LPZ440046 LPZ440549

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0156-2026%22

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