BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES

    MDR report key: 1962944 · Received December 22, 2010

    Report

    Report Number
    1831750-2010-05132
    Event Type
    Malfunction
    Date Received
    December 22, 2010
    Date of Event
    November 29, 2010
    Report Date
    November 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: BUMPER CHANNEL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WERE MISSING GREEN BUMPER STRIPS AND CHANNELS ARE BENT/FOWLER STUCK IN HIGH HEIGHT. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIVISION 0721 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA