BEUDAMED
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    CFI ULTRASOUND PROBE DRAPE

    FDA 510(k)
    FDA Class 2 ·Radiology

    WAVEWRITER ALPHA PRIME

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 14, 2023

    LONG LENGTH GAMMA NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BREAST BIOPSY DEVICE/MAGNETOM SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·May 2, 2013

    XMAX MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code ERL·September 15, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATIVE CENTER-SILICON VALLEY·Product code GEX·April 26, 2011

    Manifold Custom Kit. Label reads in part: ''CUSTOM KIT...MERIT MEDICAL''. Latex free, Sterile if package is unopened or undamaged. Part # K09-07862B, # K09-07873, #K09-02498F, #K09-07828b, #K09-00970J, #K09-06383B, #K09-07002A, #K09-04734D, #K09-00794K, and #K09-08037A.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code DQO·October 1, 2003