A Mississippi man filed a lawsuit against C.R. Bard in December 2015 alleging that the Bard Eclipse inferior vena cava (IVC) filter caused him to suffer serious injuries and permanent damage. The lawsuit, although filed in Mississippi, is expected to join others consolidated in multidistrict litigation in the District of Arizona.
After being implanted with the Bard Eclipse Filter, the plaintiff claims that he began to experience serious symptoms and returned to his doctor, who discovered that the filter had tilted to an almost horizontal position, perforating the vena cava. It had also migrated to the point of overlapping the end of the patient’s venous stent and because of complications, can no longer be removed, creating a danger that the filter’s arms and legs will eventually fracture and migrate as well.
The plaintiff makes the following allegations against Bard:
In 2010, the U.S. Food and Drug Administration (FDA) issued its first safety alert regarding the increase of adverse reports related to IVC filters, and since then, the FDA and numerous studies have uncovered a widespread failure on the part of doctors to remove these devices once they are deemed no longer necessary.
Complications associated with IVC filters include:
Besides Bard, other IVC filter manufacturers, including Cook Medical, are the subject of a rising number of product liability lawsuits alleging serious harm and death caused by these medical devices.