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Robotic Surgery Lawsuit News: Bernstein Liebhard LLP Comments on FDA Warning Letter to Intuitive Surgical Inc.
Date:7/19/2013

New York, New York (PRWEB) July 19, 2013

As robotic surgery lawsuit claims involving the da Vinci Surgical System continue to move forward in courts throughout the U.S., Bernstein Liebhard LLP comments on Intuitive Surgical Inc.’s recent disclosure that it has received a warning letter from the U.S. Food & Drug Administration (FDA) . According to a report from Bloomberg.com, the letter, dated July 17, 2013, was sent after FDA inspectors uncovered a number of issues at Intuitive Surgical’s Sunnyvale, California, headquarters this Spring.*

“Our Firm continues to receive da Vinci surgery lawsuit inquiries from patients who allegedly experienced surgical burns, excessive bleeding and other serious robotic surgery complications stemming from use of the da Vinci Surgical System. The issues detailed in the FDA’s warning letter are disturbing, and we will be monitoring these developments very carefully,” says Bernstein Liebhard LLP, a nationwide law firm representing the victims of defective drugs and medical devices. The Firm is currently offering free legal evaluations to individuals who allegedly suffered serious robotic surgery complications in procedures involving the da Vinci Surgical System.

Da Vinci Surgery Lawsuits
Launched in 2000, the da Vinci Surgical System is now used by some 1,300 U.S. hospitals for minimally invasive surgeries, according to Bloomberg.com. The FDA warning letter was issued to Intuitive Surgical following the release of a May 30th inspection report that cited the company for failing to inform the FDA about device corrections and patients who had experienced robotic surgery complications. In the letter, the FDA
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