Recall of Magnetic Resonance Imaging Systems; || Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart VANTAGE.

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Toshiba American Med Sys Inc.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    32570
  • Event Risk Class
    Class 2
  • Event Number
    Z-0986-05
  • Event Initiated Date
    2005-05-25
  • Event Date Posted
    2005-07-13
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2012-04-05
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    System, Nuclear Magnetic Resonance Imaging - Product Code LNH
  • Reason
    Patient information a is displayed with images for patient b.
  • Action
    Firm will have technicians correct each unit by visit. Instructions to them have issued.

Device

  • Model / Serial
    All.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    Magnetic Resonance Imaging Systems; || Visart, Excelart / Excelart P2 / Excelart P3 / Excelart SPIN & Excelart VANTAGE.
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Toshiba American Med Sys Inc, 2441 Michelle Dr, Tustin CA 92781
  • Source
    USFDA