PRESS RELEASE:

Bernstein Liebhard LLP, a New York law firm nationally recognized for its consumer protection and mass tort practices, is currently evaluating lawsuits related to the recent Thoratec HeartMate II pump recall. Pursuant to the Class I recall, Thoratec Corp., the manufacturer of the device, had to revise the heart pump instructions, providing a worldwide “medical device correction notification” that contained new instructions on how to properly implant the HeartMate pump. According to Reuters, Thoratec reported that it had received 29 reports of a fault in one component of the device. Five patients had to undergo additional surgeries and one patient died. The lawyers at Bernstein Liebhard are offering free and confidential case evaluations to those who received a HeartMate II pump, and suffered serious side effects or underwent additional surgeries because the pump was not properly connected.

HeartMate II Pump Recall Issued Over Defective Heart Pump Instructions

The HeartMate II pump recall was issued after Thoratec determined that a key part of the surgical procedure was omitted from the heart pump instructions, which could lead to serious side effects or death. The U.S. Food and Drug Administration (“FDA”) labeled the HeartMate II pump recall as Class I, meaning that there is a reasonable probability that use of the HeartMate pump will cause serious adverse health consequences or death. However, no product is actually being recalled and patients who have a HeartMate pump may continue to use the device. The FDA’s website states that clinicians should follow the revised heart pump instructions, which “clarify the recommended procedure for securing the bend relief to the outflow graft.”According to the Wall Street Journal, at the end of 2011, there were more than 4,000 HeartMate II patients on ongoing life-restoring support. Interestingly, former Vice President Dick Cheney had a HeartMate pump prior to his recent heart transplant.

Individuals who were implanted with a Thoratec HeartMate II pump and developed serious side effects requiring additional surgery may be entitled to compensation for medical bills, pain and suffering, lost wages and other injuries. For more information about filing a lawsuit, contact an attorney at Bernstein Liebhard LLP at (877) 779-1414 or at info@consumerinjurylawyers.com.

About Bernstein Liebhard LLP

Bernstein Liebhard LLP is a New York-based law firm exclusively representing injured persons in complex individual and class action lawsuits nationwide since 1993, including those who have been harmed by dangerous drugs, defective medical devices and consumer products. The firm has been named by The National Law Journal to the “Plaintiffs’ Hot List,” recognizing the top plaintiffs’ firms in the country, for the past nine consecutive years. Only two firms in the country have been selected for the Hot List nine years in a row.

Bernstein Liebhard LLP
10 East 40th Street
New York, New York 10016
(877) 779-1414

ATTORNEY ADVERTISING. © 2012 Bernstein Liebhard LLP. The law firm responsible for this advertisement is Bernstein Liebhard LLP, 10 East 40th Street, New York, New York 10016, (212) 779-1414. The lawyer responsible for this advertisement in the State of Connecticut is Amy L. Abate.  Prior results do not guarantee or predict a similar outcome with respect to any future matter.

Contact Information:
Felecia L. Stern, Esq.
Bernstein Liebhard LLP
info@consumerinjurylawyers.com
www.consumerinjurylawyers.com

Published April 9, 2012 by