BEUDAMED
    13 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    SCREW POSITIONING KNOB

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 23, 2023

    OPTIFLEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·April 11, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 2, 2014

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 12, 2011

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC.·Product code BZD·March 16, 2012

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 24, 2010

    REMSTAR PLUS M

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 21, 2010

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·December 1, 2010

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 26, 2011