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Da Vinci Robot Lawsuit News: Bernstein Liebhard LLP Comments on Release of FDA Warning Letter to Intuitive Surgical
Date:8/2/2013

New York, New York (PRWEB) August 02, 2013

As robotic surgery lawsuits (http://www.davincisurgery-lawsuit.com/) involving the da Vinci Surgical System mount in courts around the country, Bernstein Liebhard LLP notes that the U.S. Food & Drug Administration (FDA) has released the Warning Letter it issued to Intuitive Surgical, Inc. last month. The letter followed an FDA inspection of Intuitive Surgical’s, Sunnyvale, California headquarters, which according to Bloomberg.com, revealed that the company failed to notify the FDA about field correction letters it sent to doctors and hospitals regarding issues that had the potential to cause da Vinci complications.*

“The problems cited in the FDA Warning Letter are disturbing. It certainly raises the question of whether Intuitive Surgical was trying to conceal vital information about da Vinci complications from the FDA and the public,” says Bernstein Liebhard LLP, a nationwide law firm representing the victims of defective drugs and medical devices. The Firm is currently offering free robotic surgery lawsuit evaluations to individuals who allegedly suffered serious injuries in procedures involving the da Vinci Surgical System.

Da Vinci Surgical Lawsuits
According to the FDA Warning Letter, which was posted on the agency’s website on July 23rd, Intuitive failed to notify the agency of correction letters it sent to doctors and hospitals on several occasions. In an October 2011 correction, for example, the company notified its customers about the proper use of a Tip Cover Accessory, and advised that generators should be used with the da Vinci’s monopolar instrument. According to the FDA, Intuitive received 134 complaints of da Vinci complications related t
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3. Piece of da Vinci Surgical Robot Instrument Breaks off Inside Woman During Hysterectomy; It’s Found Following Months of Suffering, Parker Waichman LLP Notes
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