Recall of Clear Cannula System

According to Cofepris (via FOI), this recall involved a device in Mexico 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
  • Type of Event
  • Event Country
  • Event Source
    Cofepris (via FOI)
  • Event Source URL
  • Notes / Alerts
    The Mexican data is current through 2015. All of the data comes from Cofepris.
  • Extra notes in the data


  • Model / Serial
    Lot number: 214104, 214120, 214116, 214118, 214108, 214121 and 214122
  • Device Class
  • Product Description
    Instrumental Cannula System, Package with 1 and 5 pieces
  • Manufacturer


  • Source
    Cofepris (via FOI)