BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER GO BED

    MDR report key: 2213000 · Received July 12, 2011

    Report

    Report Number
    1831750-2011-06895
    Event Type
    Malfunction
    Date Received
    July 12, 2011
    Date of Event
    June 13, 2011
    Report Date
    June 13, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LUBRICATION GREASE DRIED ON SIDERAIL CAUSING LOCKING PIN NOT TO MOVE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE SIDE RAIL DID NOT LOCK PROPERLY. THERE WAS PT INVOLVEMENT; HOWEVER NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER GO BED A/C HOSPITAL BED FPO STRYKER MEDICAL 25007 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK