Field Safety Notices about 3.0T 6 Channel Flex Coil for MR750, MR750W and 3.0T HDxT (including HD23)

According to Health Sciences Authority (HSA), this field safety notices involved a device in Singapore that was produced by GE Healthcare Pte Ltd.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event ID
    600:41/01-010/15/22_36
  • Date
    2016-05-25
  • Event Country
  • Event Source
    HSA
  • Event Source URL
  • Notes / Alerts
    Data from Singapore is current through September 2018. All of the data comes from the Health Sciences Authority (HSA), 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 Singapore.
  • Extra notes in the data
    GE Medical Systems LLC

Device

  • Model / Serial
  • Product Description
    3.0T 6 Channel Flex Coil for MR750, MR750W and 3.0T HDxT (including HD23), GE Medical Systems LLC
  • Manufacturer

Manufacturer