BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PERFORMANCE PRO AMBULANCE COT

    MDR report key: 3193354 · Received June 27, 2013

    Report

    Report Number
    0001831750-2013-05856
    Event Type
    Injury
    Date Received
    June 27, 2013
    Date of Event
    May 29, 2013
    Report Date
    May 29, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO DEVICE MALFUNCTION, USER ERROR CAUSED THE EVENT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE EMT RECEIVED A BACK INJURY WHEN THE WHEEL LOCK OF THE COT WAS CAUGHT ON THE BUMPER OF THE AMBULANCE.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 EMT RECEIVED A BACK INJURY WHEN THE WHEEL LOCK OF THE COT WAS CAUGHT ON THE BUMPER OF THE AMBULANCE.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
    292035 PERFORMANCE PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1