BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TOSHIBA

    MDR report key: 2016587 · Received March 11, 2011

    Report

    Report Number
    2020563-2011-00005
    Event Type
    Injury
    Date Received
    March 11, 2011
    Date of Event
    March 1, 2011
    Report Date
    March 3, 2011
    Manufacturer
    TOSHIBA MEDICAL SYSTEMS CORPORATION
    Product Code
    JAK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TOSHIBA CUSTOMER ENGINEER (CE) IMMEDIATELY CALLED HIS MANAGER AFTER BEING STUCK WITH THE NEEDLE AND WAS DIRECTED TO GO TO THE HOSPITAL ER. THE CE GAVE THE CHARGE NURSE AT THE ER THE NEEDLE WHICH HE HAD REMOVED FROM HIS FINGER. THE CE WAS UNABLE TO BE SEEN IN THE ER AFTER SEVERAL HOURS OF WAITING, AND SAW HIS OWN PHYSICIAN THE FOLLOWING DAY FOR TREATMENT.. HE IS CURRENTLY BEING TREATED BY HIS OWN PHYSICIAN. INSPECTION OF THE DEVICE WAS NOT REQUIRED. THERE WAS NO PROBLEM WITH THE DEVICE. NO PROBLEM WITH THE DEVICE. NO PROBLEM WITH THE DEVICE.

    Description of Event or Problem · 1

    A TOSHIBA CUSTOMER ENGINEER WAS AT (B)(6) MEDICAL CENTER PERFORMING ROUTINE MAINTENANCE. WHILE CLEANING WHAT APPEARED TO BE CONTRAST OFF OF THE SYSTEM A USED NEEDLE STUCK INTO HIS FINGER APPROXIMATELY THREE FOURTHS (3/4") OF AN INCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOSHIBA COMPUTED TOMOGRAPHY SYSTEM, PRODUCT CODE: JAK JAK TOSHIBA MEDICAL SYSTEMS CORPORATION TSX-101A/HD

    Patients

    Seq Age Sex Outcome Treatment
    1 Other