One of several “bellwether” cases in a massive federal action against the maker of a transvaginal mesh device cleared an important hurdle when a judge refused to dismiss a California patient’s claim. Although the woman had her device implanted nearly three years before she sued, the evidence was conflicting regarding how long she knew about the device’s defect, which prevented the device maker from achieving dismissal based upon California’s statute of limitations.
Doctors at the Marian Medical Center in Santa Maria implanted a transvaginal mesh device into Roseanne Sanchez in early 2010 to treat her cystocele, stress urinary incontinence and pelvic organ prolapse. Almost immediately after surgery, Sanchez began noticing symptoms, including discolored discharge, itching and cramping. Despite multiple follow-up surgeries to remove portions of the mesh, the patient’s symptoms did not improve. According to Sanchez, her doctors never told her that her difficulties were the result of a defect in the device. Only after the patient saw a television commercial for transvaginal mesh litigation in 2011, and retained legal counsel, did she learn that her device was defective.
In November 2012, Sanchez joined a group of thousands of users of the device to sue the product’s maker, Boston Scientific. The manufacturer asked a federal judge to dismiss Sanchez’s case, contending that Sanchez waited too long to sue. Boston Scientific argued that the patient’s symptoms, along with her four revision surgeries, should have been enough to make her aware of her potential claim. Because each of these events occurred before November 2010, and California law gives injured people two years to sue for their injuries, the patient’s lawsuit was not timely, the company asserted in its motion.