BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 3031334 · Received March 5, 2013

    Report

    Report Number
    1824206-2013-01225
    Event Type
    Malfunction
    Date Received
    March 5, 2013
    Date of Event
    February 5, 2013
    Report Date
    February 5, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE MATTRESS TICKING WITH A REVITALIZATION KIT TO RESOLVE THE ISSUE,

    Description of Event or Problem · 1

    THE TECH ALLEGED THAT THE MATTRESS TICKING WAS WORN OUT IN CHEST AREA ALLOWING FLUID INGRESS TO THE TOP FOAM. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    94882 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1