Recall of Device Recall Sienet Magicstore

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Siemens Medical Solutions USA, 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
    37997
  • Event Risk Class
    Class 2
  • Event Number
    Z-0890-2007
  • Event Initiated Date
    2007-05-02
  • Event Date Posted
    2007-06-05
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2008-09-17
  • 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
    Digital Image Communications/Processing system - Product Code LMD
  • Reason
    System could crash and result in data loss.
  • Action
    The recalling firm issued a Safety Advisory letter to their customers (May 2, 2007) to inform them of the problem. A company representative will be contacting the customers to arrange for replacement of the RAID component.

Device

  • Model / Serial
    Model number 7502052 Serial numbers 1793, 1804, 1867, 1920, 1966, 1968, 1983, 2055, 2099, 2527, 2601, 2610, 2618, 2632, 2635, 2638, 2678, 2686, and 2689.
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    The products were shipped to medical facilities in CA, CO, FL, MS, NH, NJ, NY, and WA.
  • Product Description
    Sienet MagicStore. Radiological Digital Image Communications System
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355-1406
  • Manufacturer Parent Company (2017)
  • Source
    USFDA