Recall of FluoroSet ® Radiographic Tubal Assessment Kit, Selective Salpingography Catheter with Beacon ® Tip; Kumpe Access Catheter

According to National Organization for Medicines, this recall involved a device in Greece that was produced by Cook Incorporated.

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 all batches of medical devices: (1) FluoroSet ® Radiographic Tubal Assessment Kit, (2) Selective Salpingography Catheter with Beacon ® Tip & (3) Kumpe Access Catheter
  • Manufacturer

Manufacturer