Philips Ultrasound recalls

Recall found. Philips Ultrasound is named in FDA Class II recall Z-3249-2026 covering Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234. Hazard: 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. Identifying details: All Philips EPIQ Elite Ultrasound Systems running software version 14.0, UDI(s): (01)00884838102514 (01)00884838107540 (01)00884838114159 (01)00884838124912 (01)00884838128125. Status: Ongoing.

Models with recalls

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234 (1)

All Philips Ultrasound recalls

FDA Class II · Medical device · September 30, 2026

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234 recall — Philips Ultrasound, LLC

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

Official ID Z-3249-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.