BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EZ-PRO R4 AMBUL COT OBS (5/08)

    MDR report key: 1111931 · Received August 11, 2008

    Report

    Report Number
    1831750-2008-00108
    Event Type
    Malfunction
    Date Received
    August 11, 2008
    Date of Event
    July 13, 2008
    Report Date
    July 13, 2008
    Manufacturer
    STRYKER CORP. - MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE UNIT WAS ORIGINALLY REPAIRED INCORRECTLY CAUSING INTERFERENCE. THE CORRECT REPAIR HAS SINCE BEEN PERFORMED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE RELEASE HANDLE INTERFERES WITH THE FOWLER BRACKET.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO R4 AMBUL COT OBS (5/08) AMBULANCE COT FPO STRYKER CORP. - MEDICAL DIV. 6092000000

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK