BEUDAMED
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    Filters FDA Adverse Event ×

    REN - HARDWARE

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURING FACILITY·Product code FKX·April 26, 2010

    REN - HARDWARE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 15, 2010

    REN - HARDWARE

    FDA Adverse Event
    Death ·UNKNOWN MANUFACTURING FACILITY·Product code FKX·December 30, 2010

    REN - HARDWARE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·December 6, 2010

    REN - HARDWARE

    FDA Adverse Event
    Death ·UNKNOWN MANUFACTURING FACILITY·Product code FKX·November 30, 2010

    REN - DRUG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CASTLEBAR·Product code KPO·March 25, 2011

    REN - HARDWARE

    FDA Adverse Event
    Death ·Product code FKX·February 7, 2011

    REN - HARDWARE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 19, 2011

    REN - HARDWARE

    FDA Adverse Event
    Injury ·UNKNOWN MFG FACILITY·Product code KDI·July 9, 2009

    REN - HARDWARE

    FDA Adverse Event
    Injury ·MED-TECH INC.·Product code KDJ·September 25, 2008

    REN - HARDWARE

    FDA Adverse Event
    Injury ·MED-TECH INC.·Product code KDJ·September 25, 2008

    REN - HARDWARE

    FDA Adverse Event
    Injury ·Product code KDI·September 30, 2010

    REN - HARDWARE

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURING FACILITY·Product code FKX·September 29, 2010

    20" REN. STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·October 8, 2015

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·July 11, 2005

    PROFEMUR(R) RENAISSANCE(R) STEM

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·March 11, 2019

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 12, 2006

    REN - DISP - TWIST CLAMP/SLEEVE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·August 20, 2009

    PARIETEX

    FDA Adverse Event
    Malfunction ·SOFRADIM PRODUCTION SAS·Product code FTL·April 11, 2025

    HEARTMATE CORING KNIFE

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·July 20, 2004