Recall of EUROFLOW BT blood transfusion devices

According to National Organization for Medicines, this recall involved a device in Greece that was produced by N/A.

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
    Batch recall 130708 of EUROFLOW BT blood transfusion devices Distributor
  • Manufacturer
    N/A

Manufacturer

N/A
  • Source
    NOM