More than 95,000 Beacon Tip Angiographic Catheters have been recalled by Cook Medical, Inc.
because of a possibility that the tip may split or separate inside of patient. The U.S. Food &
Drug Administration (FDA) has categorized the Cook Beacon Tip Catheter recall a Class I medical
device recall, which indicates that there is a reasonable probability that these products could
cause serious injury or even death.
The nationwide law firm of Bernstein Liebhard LLP is now investigating potential Cook Beacon Tip
Catheter lawsuits on behalf of patients who may have been seriously injured by these products.
These individuals, or their surviving loved ones, could be entitled to compensation for medical
bills, lost wages, wrongful death and other damages associated with their injuries. If you or
someone close to you were harmed during a coronary angiogram procedure that involved the use of a
Cook Beacon Tip Catheter, please contact our attorneys today to learn more about your available