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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

inci Surgical System. On May 30th, the FDA issued a 483 letter to the company after an inspection of its headquarters revealed, among other things, that the agency had never been informed of robotic surgery complication reports that caused the company to issue a cautionary letter to its customers in October 2011.** On May 8th, Intuitive Surgical sent an Urgent Medical Device Notification to its customers after determining that micro-cracks in some EndoWrist monopolar scissors used with the da Vinci could cause surgical burns.*** Most recently, Bloomberg.com reported that sales of the da Vinci robot had slowed in the second quarter of 2013, with one analyst blaming the drop-off on hospitals “starting to re-evaluate treatment plans and taking a more cautious approach.****

Intuitive Surgical has been named in at least 26 da Vinci robot lawsuits filed on behalf of patients who allegedly suffered robotic surgery complications in da Vinci procedures. In a regulatory filing submitted to the U.S. Securities and Exchange Commission (SEC) on April 19th, Intuitive Surgical disclosed that it had entered into tolling agreements in some cases to suspend the statute of limitations, in order to give the parties more time to evaluate the claims and determine if any can be resolved out of court.*****

Victims of serious robotic surgery complications, including surgical burns, damaged organs, and torn blood vessels, that were allegedly caused by the da Vinci Surgical System may be entitled to compensation for medical bills, lost wages, and pain and suffering. To learn more about filing a da Vinci robot lawsuit, please visit Bernstein Liebhard LLP’s website. Free, no-obligation legal evaluations can also be arranged by calling 800-511-5092.

*bloomberg.com/news/2013-07-12/intuitive-surgical-may-not-have-tes
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