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FDA Safety Alert

Early Alert: Diagnostic Ultrasound System Issue from Philips Ultrasound

U.S. Food and Drug Administration
October 9, 2026
ID: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-diagnostic-ultrasound-system-issue-philips-ultrasound

FDA MedWatch Safety Alert

A software app or transducer connection problem with the Philips Lumify diagnostic ultrasound system can result in loss of or delays in scanning functionality.

Content syndicated from the official FDA MedWatch Safety Alerts and Adverse Event Reporting Program.

View Official Announcement on FDA.gov