An Indiana woman suing the manufacturer of a medical device for product liability lost when the U.S. Court of Appeals for the Seventh Circuit ruled in favor of the device manufacturer because the plaintiff failed to produce expert witness testimony on causation, as required by Indiana law in such claims.
It was a disappointing outcome, but as Indiana product liability attorneys, we recognize it’s important for attorneys – and plaintiffs too – to understand what went wrong so that we can formulate a smart strategy moving forward in similar cases. Appellate court opinions on the state and federal levels are especially important to consider because they help us gauge how courts are likely to interpret other cases in the future.
Here, according to court records, the plaintiff’s physician implanted an intrauterine device called ParaGard, made by a company named Teva. About five years after the device was implanted, the plaintiff decided she was dissatisfied with it and asked her physician to remove it. The physician did so by grasping the strings of the IUD with a ring forceps and pulling down. However, in so doing, only a piece of the device was removed. Another piece broke off either prior to or during removal, and it became lodged in her uterus. The only way to remove it, her doctors opine, is for her to undergo a hysterectomy.