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Medical Device

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

Recall date: 2026-09-30 · Source: FDA_DEVICE
Brand / Firm
Philips Ultrasound, LLC
Product
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Reason for recall
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.
Units affected
219 units
Description
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
View official recall notice →