Recall of teleflex endobronchial tubes

According to National Organization for Medicines, this recall involved a device in Greece that was produced by manufacturer #8496.

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

Device

  • Model / Serial
  • Product Description
    Recovery of batch sets of the intraocular tube Distributor
  • Manufacturer

Manufacturer