BEUDAMED
    FDA Adverse Event Injury Summary report: N

    POWER PRO AMBULANCE COT

    MDR report key: 757170 · Received August 25, 2006

    Report

    Report Number
    1831750-2006-00050
    Event Type
    Injury
    Date Received
    August 25, 2006
    Date of Event
    July 28, 2006
    Report Date
    July 28, 2006
    Manufacturer
    STRYKER CORP, MED. DIV.
    Product Code
    FPO
    Removal / Correction Number
    1831750-2006-003C
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTEDLY, THE BOLTS BACKED OUT FROM THE LOAD WHEEL CASTING. ALLEGEDLY, THE EMT STRAINED HIS BACK. REPORTEDLY, HE RECEIVED PRESCRIPTION MEDICATION AND WAS PLACED ON WORKMEN'S COMPENSATION. NO ADVERSE CONSEQUENCES TO THE PATIENT HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POWER PRO AMBULANCE COT AMBULANCE COT FPO STRYKER CORP, MED. DIV. 6500000000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention