BEUDAMED
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    I OPEN 0.5T

    FDA 510(k)
    FDA Class 2 ·Radiology

    CANALIZER HYDROPHILIC GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RANDOX AMMONIA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    VITAGEL 4.5ML

    FDA Adverse Event
    Injury ·STRYKER ORTHOBIOLOGICS-MALVERN·Product code LMF·May 2, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·September 15, 2014

    TRIATHLON #5 CR INSERT 9MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·May 12, 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