BEUDAMED
    FDA Enforcement Class III Ongoing

    S3-1 Transducer Probe

    Recall: Z-2390-2025 · Reported September 3, 2025

    Enforcement

    Recall Number
    Z-2390-2025
    Event ID
    97217
    Classification
    Class III
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Philips Ultrasound, Inc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    September 3, 2025
    Initiation Date
    July 3, 2025
    Classification Date
    August 22, 2025
    Address
    1 Echo Dr, Reedsville, PA, 17084-8603, United States

    Description

    S3-1 Transducer Probe

    Reason

    To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

    Code Info

    Model No. 989605387381, 989605361403, 989605440732, 989605361401; UDI: (01)00884838068001(21)B1RDXB, (01)00884838068001(21)B1RQG6, (01)00884838068001(21)B1RMV9, (01)00884838067608(21)B1YRPX, (01)00884838067608(21)B1YT4J, (01)00884838068001(21)B24RFX, (01)00884838068001(21)B1RDX8, (01)00884838068001(21)B20PGC, (01)00884838068001(21)B1RJT1, (01)00884838068001(21)B20PGB, (01)00884838068001(21)B1RDNY, (01)00884838068001(21)B1MW4N, (01)00884838068001(21)B1MVVJ, (01)00884838068001(21)B20PN8, (01)00884838068001(21)B1RDXC; Serial No. 0388D2, B1JWWV, B19RZV, B0RHV4, B0RH23, B1RDXB, B16W47, B1RQG6, B0RHV3, B19QZZ, B19R10, B16JPL, B1RMV9, B19V6V, B1YRPX, B1YT4J, B24RFX, B0RHV1, B0RR1C, B19V02, B10DQ0, B19V08, B1RDX8, B20PGC, B1RJT1, B20PGB, B1JWWZ, B1RDNY, B1MW4N, 03DLPH, B19V05, B19V6N, B1MVVJ, B0RHV5, B0RHV8, B20PN8, B1RDXC, B19V6W, B0RHV2.

    Distribution

    US Nationwide distribution.

    Quantity

    171,322 units