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    FDA Recall: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Interventional Fluoroscopic X-Ray System

    Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

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    FDA
    infoPhilips

    Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

    Device class: 2

    Device name: Interventional Fluoroscopic X-Ray System

    Event initiated: 2026-06-17

    FDA posted: 2026-08-05

    Recall ID: Z-2893-2026

    Product: Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400.

    Interventional Fluoroscopic X-Ray System.

    Reason for recall

    Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

    Citations
    #recall
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