Events

Recall of X-ray fluoroscopy for stationary digital circulators, X-ray fluoroscopy for stationary digital circulators, X-ray fluoroscopy for stationary digital circulators, X-ray fluoroscopy for stationary digital circulators, Angiographic X-ray devices, Stationary digital circulation X-ray fluoroscopy device, X-ray fluoroscopy device for stationary digital circulator, X-ray fluoroscopy device for stationary digital circulator

According to Korean Food & Drug Administration, this recall involved a device in South Korea that was produced by Siemens Co., Ltd..

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
    88
  • Date
    2014-05-21
  • Event Country
    South Korea
  • Event Source
    KFDA
  • Event Source URL
    https://emed.mfds.go.kr
  • Notes / Alerts
    Korean data is current through September 2018. All of the data comes from Korean Food & Drug Administration, 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 South Korea.
  • Extra notes in the data
    Acquisition 07-553, Acquisition 08-484, Acquisition 08-796, Acceptance 09-197, Acceptance 09-149, Acceptance 05-374, Acceptance 05-713, Acceptance 06-543

Device

X-ray fluoroscopy for stationary digital circulators, X-ray fluoroscopy for stationary digital ci...

Manufacturer

Siemens Co., Ltd.
  • Manufacturer Address
    23, Chungjeong-ro, Seodaemun-gu, Seoul
  • Manufacturer Parent Company (2017)
    Siemens AG
  • Source
    KFDA