Designed to prevent life-threatening strokes, Inferior Vena Cava (IVC) filters are supposed to protect patients from dangerous blood clots. However, these defective devices have been linked to serious injuries or death. The defective product attorneys at the law offices of O'Connor, Acciani and Levy are experienced in handling dangerous product litigation. Our Cincinnati Bard IVC filter lawyers can help you seek compensation through a class action lawsuit if you or someone you love was injured because of this dangerous device. Our firm offers free legal consultations and can help you determine your legal options. We also work on a contingency fee basis and do not get paid unless you recover a verdict or settlement.
FRACTURE / EMBOLIZATION WARNING SIGNS
IVC filters have been linked to a number of potentially life-threatening side effects. The IVC filter is a small, spider-like shaped implant that works by trapping blood clots before they can travel to vital organs such as the lungs or heart. If these clots travel to the lungs, they can form a life-threatening pulmonary embolism. A pulmonary embolism can occur when blood clots travel through the bloodstream and become lodged near the lung. This can cause a sudden blockage of the artery that brings blood into the lungs, causing serious and potentially fatal injuries. A problem linked to Bard IVC Filters is the possibility that they might fracture. The struts or legs of the filters can break off and migrate from the vena cava to other parts of the body, including vital organs such as the heart or lungs, leading to fatal injuries, which may include:- Hemorrhage
- Cardiac/pericardial tamponade
- Chronic excruciating pain
- Perforation of vital tissue, vessels or organs
- Death
FDA IVC FILTER WARNINGS
If you are at risk of developing life-threatening blood clots, you might have agreed to insert this device so you could save your life. That decision could kill you. Since 2005, the Food and Drug Administration(FDA) has received over 900 adverse event reports involving Inferior Vena Cava filters. The FDA received reports of:- Device migrations
- Embolizations or detachment of the device components
- IVC perforations
- IVC filter fractures