Recall of Dispositif d’insertion manuel EZIO

According to Republic of Lebanon Ministry of Public Health, this recall involved a device in Lebanon that was produced by Teleflex Medical.

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



  • Manufacturer Parent Company (2017)
  • Manufacturers representative
    INTERMEDIC S.A.L./PRIMEmedical/Biomedic S.A.R.L.
  • Source