Medtronic issues recall diabetes software affecting CareLink version 4.2B due to incorrect glucose data display, prompting clinician review.

Medtronic has issued a warning about rapid unexpected battery depletion that may happen in seven kinds of implantable defibrillators, affecting nearly 340,000 implanted devices worldwide. The Food and ...

The FDA alerted health care providers to another potential issue with Medtronic's HeartWare Ventricular Assist Device this week, saying a welding defect may cause it to malfunction. Medtronic notified ...

MINNEAPOLIS (AP) - Medical device maker Medtronic is warning patients about a rare problem with its SynchroMed drug pumps that can cause them to lose battery power and fail. The company says it has ...

A month after acquiring the LVAD maker for $1.1 billion, Medtronic says FDA has designated two of its recalls as Class I. Maureen Kingsley Medtronic says it is making some important manufacturing ...

MINNEAPOLIS (WCCO) --A consortium of investigative journalists has published a report indicating that, in the last decade, Twin Cities-based Medtronic medical devices have been connected with more ...

Note: This story has been updated throughout with additional information. Following a patient death, the U.S. Food and Drug Administration is warning about a rare battery depletion problem in certain ...

Medtronic has issued a second alert letter to patients regarding shortened battery life of the MiniMed 600 and 700 series insulin pumps. The affected products include the MiniMed 630G, 670G, 770G, and ...