BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 2001796 · Received February 3, 2011

    Report

    Report Number
    1831750-2011-01048
    Event Type
    Malfunction
    Date Received
    February 3, 2011
    Date of Event
    December 27, 2010
    Report Date
    January 5, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A TRANSPORTER SUSTAINED A BACK STRAIN WHILE PUSHING A 2040 ZOOM PRODUCT. THE TRANSPORTER WAS NOT EXAMINED BY A PHYSICIAN AND DID NOT RECEIVE MEDICAL INTERVENTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOOM CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 2040 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK