BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HILL-ROM 405 ELECTRIC BED

    MDR report key: 2932434 · Received January 14, 2013

    Report

    Report Number
    3006697241-2013-00011
    Event Type
    Malfunction
    Date Received
    January 14, 2013
    Date of Event
    December 17, 2012
    Report Date
    December 17, 2012
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE CARDIO PULMONARY RESUSCITATION CABLE WAS THE CAUSE OF THE ISSUE. THE ACCOUNT REPLACED THE CARDIO PULMONARY RESUSCITATION CABLE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE CARDIO PULMONARY RESUSCITATION DOES NOT FUNCTION. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    21282 HILL-ROM 405 ELECTRIC BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 1440B

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK