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Da Vinci Robotic Surgery Lawsuit Update: Wright & Schulte LLC Disturbed by Research Indicating Da Vinci Surgery Complications May Be Underreported
Date:9/8/2013

more information on filing a Da Vinci robot lawsuit, or to arrange for a free legal consultation, please visit yourlegalhelp.com.
[sec.gov/Archives/edgar/data/1035267/000119312513297410/d551118d10q.htm; SEC, July 22, 2013]

The Da Vinci Surgical System was launched by Intuitive Surgical in 2000, and is the only robotic surgery platform approved by the FDA for use in soft tissue procedures. According to a recent Bloomberg News report, the device has been associated with a growing number of adverse event reports, which prompted the FDA to launch a survey of doctors who use the robot earlier this year. Among other things, the agency is seeking information on the types of Da Vinci robot complications physicians may have observed.
[bloomberg.com/news/2013-03-21/intuitive-robosurgery-training-seen-lacking-in-lawsuits.html, Bloomberg, March 21, 2013]

According to Wright & Schulte LLC, the newly-published Johns Hopkins study is just the most recent development to raise questions about the safety of the Da Vinci robot. In May, Intuitive Surgical warned its customers about an issue with its EndoWrist Monopolar Curved Scissors that could cause surgical burns in patients. In July, the company was sent an FDA Warning Letter after an inspection of its headquarters turned up several issues, including problems with the way it reported Da Vinci complications to the agency. That same month, Intuitive Surgical announced a recall for some Da Vinci instruments that may not have been properly tested at the factory.
[fm.cnbc.com/applications/cnbc.com/resources/editorialfiles/2013/05/10/UrgentDaVinci.pdf, Intuitive Surgical, May 8, 2013]
[fda.gov/ICECI/EnforcementActions/WarningLetters/2013/ucm363260.htm, FDA, July 16, 2013]
[bloomberg.com/news/2013-07-12/intuitive-surgical-may-not-have-tested-devices-properly.ht
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