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Recall Observatory FDA recall evidence

Device product

EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232

Z-0123-2022

September 21, 2021

Class II

Product summary

Firm
Philips Ultrasound Inc
Event
Event 88728
Status
Terminated
Classification
Class II
Quantity
107
Official record key
device-enforcement:Z-0123-2022

Official wording

Reason: 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.

Code information: Software Versions: 6.0, 7.0, 7.0.3

Distribution pattern: US: MI, AZ, IA, TN, OH, CO, WI, NY, NJ, NC, LA, IL, CA, KY, IN, MD, TX, PA. OUS: Denmark, Latvia, Belgium, Hungary, Argentina, Canada, Spain, Germany, Greece, Korea, Republic of Japan, France, Australia, Egypt, Switzerland, Italy, Senegal, Israel, Indonesia, Netherlands, Hong Kong, United Kingdom, Poland, Finland, India, New Zealand

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software issue can cause an EchoNavigator error