FDASeptember 21, 2021device

EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232

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

The hazard

Ultrasound system software issue can cause an EchoNavigator error notification, leading to an unresponsive system, necessitating system restart, which could lead to therapy/treatment delay and/or unnecessary therapy/treatment. Can occur during ultrasound-guided TEE with EchoNavigator, if secondary screen capture is enabled and user presses other system buttons before secondary capture completed.

What to do

FDA enforcement status: Terminated

Brands named

philips ultrasoundphilips

Recall history

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

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