BEUDAMED
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    IMMUNOSORBA COLUMN

    FDA Adverse Event
    Injury ·FRESENIUS HEMOCARE·Product code LQQ·February 3, 2006

    PYXISES REF 13CF, LHG-6DEEP,3STDBINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 27, 2025

    PYXISES REF5CF,LHG-3DEEP,3STDBINS,CASTER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 31, 2025

    PYXISES REF 13CF, LHG-3DEEP,9STDBINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 22, 2025

    PYXISES REF 13CF, LHG-3DEEP,9STDBINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 30, 2025

    PYXISES REF 5CF, LHG-3DEEP,3STDBINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 30, 2025

    PYXISES REF 13CF, LHG-6DEEP,3STDBINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 12, 2025

    PYXISES REF 5CF, LHG-12 STD BINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 13, 2025

    PYXISES REF 5CF, LHG-6 STD BINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 24, 2025

    PYXISES REF 5CF, LHG-9 STD BINS

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 5, 2025

    PYXISES REF 5CF, LHG-9 STD BINS, CASTER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 22, 2025

    PYXISES REF 5CF, LHG-6 STD BINS, CASTER

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 30, 2025

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·September 17, 2025

    BD PYXIS¿ ES REFRIGERATOR

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 30, 2025

    LEAD DELIVERY SYS, 13 CM (5 IN), 1 EACH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LHG·September 24, 2015

    LEAD DELIVERY SYS, 19CM (7.5 IN), 1 EACH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LHG·September 24, 2015

    LEAD DELIVERY SYS, 19CM (7.5 IN), 1 EACH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LHG·September 24, 2015

    ITREL

    FDA Adverse Event
    Other ·NEURO·Product code LHG·December 11, 2003

    EPIDURAL CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT LABORTORIES·Product code LHG·June 30, 1992

    SYMMIX

    FDA Adverse Event
    Other ·MEDTRONIC, INC.·Product code LHG·August 19, 1997