BEUDAMED
    FDA Adverse Event Other Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 2141546 · Received June 17, 2011

    Report

    Report Number
    1831750-2011-06088
    Event Type
    Other
    Date Received
    June 17, 2011
    Date of Event
    June 3, 2011
    Report Date
    June 3, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE IN FASTENER SHUT OFF WAS INSTALLED INCORRECTLY AND WAS IN THE WAY OF THE UNIT AND DID NOT ALLOW THE COT TO LOCK INTO THE RAIL ASSEMBLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE COT WAS UNABLE TO LOCK INTO THE RAIL ASSEMBLY BECAUSE THE IN FASTENER SHUT OFF WAS INSTALLED INCORRECTLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT STRETCHER, WHEELED INK STRYKER MEDICAL 6500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1