Results 1 to 1 of 1
11-01-2010, 03:00 PM #1
FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall
Medtronic, Inc. (NYSE: MDT) today announced the U.S. Food and Drug Administration (FDA) has classified the company's previous action related to the Octopus® Nuvo Tissue Stabilizer as a Class I recall. FDA classifies a recall as Class I when the agency believes that there is a reasonable probability that use of the recalled product will cause serious adverse health consequences or death.