BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1123308 · Received August 20, 2008

    Report

    Report Number
    1824206-2008-00871
    Event Type
    Malfunction
    Date Received
    August 20, 2008
    Date of Event
    August 22, 2006
    Report Date
    August 22, 2006
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN 2007 - REPORTER REPORTED THAT SHE HAS 28 BEDS THAT THE SIDERAILS DO NOT LATCH. SHE REQUESTED 28 INLINE SIDERAIL LATCH KITS. I PLACED AN ORDER FOR 50 SIDERAIL UPGRADE KITS SO SHE HAD SOME STOCK. SHE INSTALLED VERSACARE SIDERAIL INLINE SPRING KIT, AND THE SIDERAIL LATCHED PROPERLY. SHE DID NOT RECORD THE BED SERIAL NUMBER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1