Recall database

System, Imaging, Pulsed Doppler, Ultrasonic recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIOngoingZ-3249-2026

Philips Ultrasound, LLC recalls Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow velocity measurements and misdiagnosis.

Ultrasonic Pulsed Doppler Imaging System
Software Design Change

Philips Ultrasound, LL…WASep 30, 2026

Class IICompletedZ-1007-2026

Philips Ultrasound, LLC recalls Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c tr…

Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.

Ultrasonic Pulsed Doppler Imaging System
Software Design Change

Philips Ultrasound, LL…WAJan 7, 2026