BEUDAMED
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    Filters FDA Adverse Event ×

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·June 13, 2014

    UNKNOWN ZIMMER HIP

    FDA Adverse Event
    Malfunction ·ZIMMER INC.·Product code JDI·October 12, 2010

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 13, 2012