Philips Lumify Ultrasound Recalled After Four Patient Deaths

Philips recalls Lumify point-of-care ultrasound after software bug forces unexpected re-registration, blocking scans; linked to four deaths and eight serious injuries. FDA warns delays in remote settings without backup may cause serious harm.

• The recall affects Lumify diagnostic ultrasound systems running iOS 2.X, 5.0, 5.1.2, 5.1.3 and Android 1.X, 3.X, 4.X, 5.1, 5.1.1 app versions.
• The software issue prevents recognition of a previously registered account, halting scanning until re-registration is completed; USB connection instability may also occur.
• Until a software update is available, users should only operate the system with reliable Wi-Fi/cellular or have an alternative imaging plan, especially in ambulances, aircraft, or field settings.

Automated summary

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