BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED+

    MDR report key: 1950912 · Received November 5, 2010

    Report

    Report Number
    9680128-2010-00272
    Event Type
    Malfunction
    Date Received
    November 5, 2010
    Date of Event
    October 12, 2010
    Report Date
    October 12, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE BRAKES DID NOT WORK ON THE HEAD END AND THE POWER CORD IS MISSING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ HOSPITAL BED, A-C POWERED ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK