FDAAugust 6, 2021device

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205 EPIQ 5G - 795204 EPIQ 7 - 795117 EPIQ 7C - 795201 EPIQ 7G - 795200 EPIQ CVxi -795232 EPIQ CVx - 795231

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.

What to do

FDA enforcement status: Completed

Brands named

philips ultrasoundphilips

UPCs

008848380476860088483808865800884838047693

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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