June 27, 2006 — The US Food and Drug Administration (FDA) and Guidant Cardiac Rhythm Management (a Boston Scientific company) have notified healthcare professionals via letter regarding the potential ...

WASHINGTON - A serious software problem with two models of automatic external defibrillators has led their manufacturer to recall thousands of the devices distributed worldwide. Defibtech LLC said ...

WASHINGTON (AP) -- A malfunction in some of the Guidant Corp. defibrillators recalled last month could cause serious injury or death, the government said Friday in classifying 20,000 of the devices as ...

The North American subsidiary of Amsterdam-based Royal Philips reached an agreement on a consent decree with the U.S. Department of Justice, representing the Food and Drug Administration, the company ...