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Medical Device

Philips Lumify Diagnostic Ultrasound System

Recall date: 2026-10-28 · Source: FDA_DEVICE
Brand / Firm
Philips Ultrasound, LLC
Product
Philips Lumify Diagnostic Ultrasound System
Reason for recall
Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be unavailable outside of the hospital (ambulances/aircraft/field); 2) At connection between transducer USB cable to tablet/phone, there may be an unstable connection/may disconnect disrupting function. May cause diagnosis/treatment delay.
Units affected
13,206
Description
Philips Lumify Diagnostic Ultrasound System
View official recall notice →