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Da Vinci Robot Lawsuit News: Bernstein Liebhard LLP Comments on Class II Recall for Da Vinci Robot Instruments
Date:7/15/2013

New York, New York (PRWEB) July 15, 2013

As da Vinci robot lawsuit claims continue to move forward in courts throughout the country, Bernstein Liebhard LLP notes that Intuitive Surgical, Inc. has announced a Class II recall for certain instruments used with the da Vinci Surgical System. According to a Bloomberg.com report published on July 12th, the recall for the da Vinci Si Vision System Cart, Si Surgeon Side Cart, Instrument Control Box and Dual Camera Controller has been given Class II status by the U.S. Food & Drug Administration (FDA), which indicates the products “may cause temporary or medically reversible adverse health consequence.”*

“Our Firm continues to receive inquiries from victims of robotic surgery complications that were allegedly caused by the da Vinci Surgical System. We expect that this recall will only add to the safety concerns that already surround this device,” 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 Robot Lawsuits
Launched in 2000, the da Vinci Surgical System was used in some 400,000 minimally invasive surgeries last year, according to Bloomberg.com. According to an Urgent Device Correction notice Intuitive Surgical sent to its affected customers on June 27th, the da Vinci robot instruments subject to this recall may not have been tested properly at the factory. All of the instruments have been retested in the field, and the company has not received any complaints connected to the products, Bloomberg.com said.

The last few months have been difficult ones for Intuitive Surgical and the da V
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