BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRIME ZOOM STRETCHER, ELECTRIC

    MDR report key: 3233159 · Received July 18, 2013

    Report

    Report Number
    0001831750-2013-06449
    Event Type
    Injury
    Date Received
    July 18, 2013
    Date of Event
    June 18, 2013
    Report Date
    June 19, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    INK
    PMA / PMN Number
    K022309
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    MANUFACTURER'S INVESTIGATION IS ONGOING. IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT MAY BE SUBMITTED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT DURING PATIENT TRANSPORT THE STRETCHER STOPPED WORKING. NURSE ALLEGEDLY INJURED HER KNEE AS A RESULT OF THE ZOOM DRIVE DISENGAGING DURING USE. CUSTOMER REPORTED THAT THE NURSE REQUIRED MEDICAL INTERVENTION AS A RESULT OF THE INCIDENT. CUSTOMER AND THE STRYKER TECHNICIAN EVALUATED THE UNIT AND WERE NOT ABLE TO DUPLICATE THE ALLEGED FAILURE OF THE ZOOM DRIVE DISENGAGING DURING USE. NO ADDITIONAL INFORMATION ON THE NURSE'S INJURY WAS MADE AVAILABLE AT THIS TIME BY THE CUSTOMER. MANUFACTURER'S INVESTIGATION IS ONGOING. IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT MAY BE SUBMITTED. NO ADVERSE CONSEQUENCES WERE REPORTED ON BEHALF OF THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    333689 PRIME ZOOM STRETCHER, ELECTRIC STRETCHER, WHEELED, POWERED INK STRYKER MEDICAL-KALAMAZOO 1125E

    Patients

    Seq Age Sex Outcome Treatment
    1