BEUDAMED
    FDA Adverse Event Summary report: N

    MANUAL PATIENT ROTATION BED

    MDR report key: 2871085 · Received December 12, 2012

    Report

    Report Number
    1531186-2012-01728
    Date Received
    December 12, 2012
    Report Date
    December 12, 2012
    Manufacturer
    UNKNOWN
    Product Code
    FNJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    (B)(4). THE DEALER REPORTED THAT THE 7714P TRAPEZ HOMECARE BED HAD ONE BENT LEG. THERE WAS NO PATIENT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MANUAL PATIENT ROTATION BED 890.5180 FNJ UNKNOWN 7714P

    Patients

    Seq Age Sex Outcome Treatment
    1 Other