Recall of Device Recall 3D TOP Ceiling Stand

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
    34191
  • Event Risk Class
    Class 2
  • Event Number
    Z-0335-06
  • Event Initiated Date
    2005-11-30
  • Event Date Posted
    2005-12-31
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2006-07-19
  • 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
    Tube Mount, X-Ray, Diagnostic - Product Code IYB
  • Reason
    Screws on the rollers may become loose.
  • Action
    The recalling firm has issued a field correction per Update Instructions AX004/06/S. This update instructs a Siemens Customer Service Engineer to visit affected consignees and checkthe screws on the rollers. It also provides roller bearing sleeves as a secondary safety mechanism to prevent the rollers from detaching.

Device

  • Model / Serial
    Model number 8773673
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    The products were shipped to hospitals and medical facilities nationwide.
  • Product Description
    3D TOP Ceiling Stand. X-Ray System model number 8773673
  • Manufacturer

Manufacturer

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