BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

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

    MDR report key: 1823284 · Received August 27, 2010

    Report

    Report Number
    1831750-2010-01926
    Event Type
    Malfunction
    Date Received
    August 27, 2010
    Date of Event
    July 31, 2010
    Report Date
    July 31, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE COT DID NOT LOCK AND COLLAPSED WITH A PT ON IT. NO ADVERSE CONSEQUENCE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EZ-PRO R4 AMBUL COT OBS(5/08) STRETCHER WHEELED FPO STRYKER CORP., MEDICAL DIV. 6092 NA

    Patients

    Seq Age Sex Outcome Treatment
    1