Recalls for Medtronic, Inc.

FDA Classifies Medtronic's Worldwide Voluntary Field Action on Guidewires as Class I Recall
11/16/2013 Food Recall

Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified the company's recently initiated voluntary field action related to certain guidewires as a Class I recall. Based on an internal investigation following a limited number of complaints, including one patient injury, Medtronic began notifying hospitals and distributors worldwide the week of Oct. 21 that some models of its guidewires from recent lots have the potential for the coating on their surface to delaminate and detach.

  • Company:
    Medtronic, Inc.
  • Problem
    Have the potential for the coating on their surface to delaminate and detach
Medtronic Issues Medical Device Notifications Regarding The Synchromed Implantable Infusion System
06/28/2013 Food Recall

June 26, 2013 - MINNEAPOLIS – In June 2013, Medtronic, Inc. (NYSE: MDT) initiated four medical device notifications to customers worldwide about the SynchroMed Implantable Infusion System. These notifications provide clinicians with information to help identify and manage issues that impact the safe and reliable delivery of therapy using the SynchroMed Implantable Infusion System.

  • Company:
    Medtronic, Inc.
  • Problem
    Undeclared Milk, Soy And Wheat