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Philips Lumify Systems — recall 81284

Health Canada — Medical Devices · Canada · 2025-11-26 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 81284
Date of alert: 2025-11-26
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Radiology - Cardiovascular
Product type: Medical devices

Reported risk: Philips has become aware that the Lumify system is incompatible with Apple devices that have USB-C connector and are running iOS 18, which will cause a failure to perform live imaging potentially resulting in the procedure needing to be redone or rescheduled.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/philips-lumify-systems

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Philips Lumify Systems — recall 81284

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