Law360 quoted Blackwell Burke P.A. Partner Peter J. Goss in an article published today discussing a recent physician’s medical device error report to the U.S. Food and Drug Administration. The physician reported that the wiring of an implanted heart device broke through the device’s insulation. Mr. Goss commented on how media coverage increases physician surveillance and reporting of suspected errors in recalled and non-recalled products. The full article is available here.
Mr. Goss focuses his national practice on pharmaceutical and medical device product liability litigation and toxic torts. He has represented major pharmaceutical, medical technology, and chemical firms in hundreds of cases. Mr. Goss, who has won several published Daubert decisions, often serves as “science counsel” in life sciences litigation. He collaborates with leading experts to present complex medical and scientific evidence, both in dispositive motions and at trial. He is a frequent commentator on scientific evidence and legal developments of interest to FDA-regulated industries.
Blackwell Burke P.A., a litigation and trial boutique in Minneapolis, Minnesota, serves as national trial and litigation counsel for numerous Fortune 500 companies. The firm has extensive experience in class action defense, commercial litigation, food industry defense, labor and and employment, and products liability. The firm has represented corporate clients in practically every jurisdiction in the country, as well as several foreign countries.
For more information about Blackwell Burke P.A. or Mr. Goss, please contact Kandy Branch at 612-343-3235.