BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3130350 · Received March 12, 2013

    Report

    Report Number
    3006697241-2013-00051
    Event Type
    Malfunction
    Date Received
    March 12, 2013
    Date of Event
    February 11, 2013
    Report Date
    February 11, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT FOUND THE SIDE RAIL LATCH IS BENT AND THE SIDE RAIL LATCH SCREW, NUT AND BUSHING ARE MISSING. THE ACCOUNT REPLACED THE SIDE RAIL LATCH SCREW, BUSHING AND NUT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    104522 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV

    Patients

    Seq Age Sex Outcome Treatment
    1