Recall of Ultrasonic surgical handpiece tip, single-use

According to National Organization for Medicines, this recall involved a device in Greece that was produced by Ethicon Endo-Surgery LLC (USA).

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
    Recall of the total batches of the medical device "Ultrasonic surgical handpiece tip, single-use"
  • Manufacturer

Manufacturer