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On July 2, the FDA announced that Medtronic Duet External Drainage and Monitoring System is recalled (Class I).
The move leaves uninterrupted a federal appeals court decision, enabling the action to proceed. Port Washington, New York (PRWEB) June 25, 2014 Parker
The largest stand-alone medical device manufacturer in the world has revealed that hackers had successfully infiltrated its computers, and that it had lost some patient records in separate incidents last year.
Another Medtronic Infuse Lawsuit Accuses The Manufacturer of the Infuse Bone Graft For Promoting Use In Non-FDA -Approved Surgical Procedures, Coaching Doctors and Misrepresentation.
The $9.9 million settlement is meant to resolve allegations made under the False Claims Act that Medtronic engaged in kickback schemes to increase sales of its pacemakers and defibrillators.
Editor Note: For more information about this release, please scroll to bottom. NEW YORK, May 15, 2014 /PRNewswire/ -- Today, Analysts Review released its analysts'
Editor Note: For more information about this release, please scroll to bottom. NEW YORK, April 28, 2014 /PRNewswire/ -- Today, Analysts Review released its analysts'
A Motion to Remand Has Been Granted by a Federal Court in A Case Brought Against Medtronic, Inc. and Medtronic Sofamor Danek USA, Inc. Over its InFUSE™ Bone Graft Product.
SAN ANTONIO, March 11, 2014 /PRNewswire/ -- Aperion Biologics, Inc., a clinical-stage regenerative medical device company, announced that France Dixon Helfer and Mike Ward were appointed to
- Of or relating to good digestion.