Recall of HOYA intraocular models

According to National Organization for Medicines, this recall involved a device in Greece that was produced by HOYA Surgical Optics.

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


  • Model / Serial
  • Product Description
    Recall of specific HOYA intraocular models
  • Manufacturer