BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 3172468 · Received June 17, 2013

    Report

    Report Number
    0001831750-2013-05460
    Event Type
    Malfunction
    Date Received
    June 17, 2013
    Date of Event
    May 19, 2013
    Report Date
    May 21, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE LITTER LOCKING MECHANISM EXTENSION SPRINGS WERE REPLACED AS A PRECAUTION, AS THE CUSTOMER ALLEGED THAT THE ISSUE COULD BE AN INTERMITTENT ISSUE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT DROPPED WHILE TRANSPORTING A PATIENT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT DROPPED WHILE TRANSPORTING A PATIENT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    273907 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1