Medtronic Recalls 48 Implantable Cardiac Defibrillators Due to Manufacturing Error

A manufacturing error has resulted in a Class I recall of Medtronic implantable cardiac defibrillators. The U.S. Food and Drug Administration (FDA) warns consumers that using the recalled devices could result in serious injury or death. Read on to learn more about the recalled products, and what you should do if you are impacted by… Read More