BEUDAMED
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    GOLDEN LIFT CHAIR WITH FIR HEAT

    FDA Adverse Event
    Injury ·GOLDEN TECHNOLOGIES·Product code INO·October 1, 2012

    LIGHTMIX ZIKA RRT-PCR TEST (EUA)

    FDA Adverse Event
    Malfunction ·OLFERT LANDT, TIB MOLBIOL SYNTHESELABOR GMBH·Product code POA·March 9, 2017

    LIGHTMIX ZIKA RRT-PCR TEST (EUA)

    FDA Adverse Event
    Malfunction ·OLFERT LANDT, TIB MOLBIOL SYNTHESELABOR GMBH·Product code POA·March 9, 2017

    TRUSCAN BODY COMPATIBLE WITH HIOSSEN (OSSTEM) ET (TS) REGULAR

    FDA Adverse Event
    Malfunction ·TRUABUTMENT KOREA CO., LTD.·Product code NDP·February 4, 2025

    CARDIOSAVE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·June 3, 2014

    SECUR-FIR HA PSL CUP/CLUSTR SHELL 70MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·June 24, 2010

    ZIMMER M/L PRESSW-FIR TAPER FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LZO·August 8, 2012

    ELLIPSE VR ICD, US

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. (CRM-KISTA)·Product code LWS·September 2, 2015

    SENSATION PLUS UNK.VOL

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DSP·July 10, 2017

    BLOOD MONITOR PUMP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORP·Product code FIR·March 19, 2002

    3002807350-2007-00001

    FDA Adverse Event
    Death ·Product code FIR·February 2, 2007

    ACCURA HEMOFILTRATION SYSTEM

    FDA Adverse Event
    Malfunction ·MESYS·Product code FIR·November 27, 2007

    BAXTER

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP. RENAL PRODUCT SVC·Product code FIR·February 2, 2001

    ACCURA HEMOFILTRATION SYSTEM

    FDA Adverse Event
    Malfunction ·MESYS GMBH- MEDIZINISCHE SYSTEME·Product code FIR·May 19, 2008

    BM14 FLUID UF MODULE FOR BM25

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES GERMANY GMBH·Product code FIR·June 22, 2011

    ACCURA HEMOFILTRATION SYSTEM

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE·Product code FIR·January 11, 2008

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·July 9, 2013

    AMK CEM FIX STEM TIB TRAY

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·March 15, 2002

    VAS-CATH SOFT-CELL KIT 12.5 F X 23 CM (PRE-CURVED LONG TERM)

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code LFJ·January 30, 2013

    TRIGEN FEMORAL INTRAMEDULLARY NAIL

    FDA Adverse Event
    Malfunction ·SMITH AND NEPHEW, INC.·Product code JDS·February 28, 2022