Events

Recall of STILLE SONESTRA VIDEO FLUOROSCOPY TABLE 6210

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by STILLE AB.

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
    35511
  • Event Risk Class
    II
  • Event Initiated Date
    2008-10-23
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    A short circuit may lead to a malfuction in the control box. this can result in an uncontrolled movement of the table which cannot be stopped by disconnecting the device from the main power supply.

Device

STILLE SONESTRA VIDEO FLUOROSCOPY TABLE 6210
  • Model / Serial
    Model Catalog: (Lot serial: )
  • Product Description
    Stille Sonestra 6210 Fluoroscopy Table
  • Manufacturer
    STILLE AB

Manufacturer

STILLE AB
  • Manufacturer Address
    TORSHALLA
  • Manufacturer Parent Company (2017)
    Linc AB
  • Source
    HC