BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    6083 AMBULANCE COT

    MDR report key: 2191598 · Received July 1, 2011

    Report

    Report Number
    1831750-2011-06689
    Event Type
    Malfunction
    Date Received
    July 1, 2011
    Date of Event
    June 6, 2011
    Report Date
    June 6, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    AT FILING DATE, NO ADD'L DETAILS ARE KNOWN. A F/U WILL BE ISSUED AS NECESSARY BASED UPON INVESTIGATION RESULTS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY EMAIL THAT A (B)(4) COT DROPPED. THE EMAIL DID NOT INDICATE IF THERE WAS A PT INVOLVED OR IF THERE WERE ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 6083 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL 6083 NA

    Patients

    Seq Age Sex Outcome Treatment
    1