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MicroPort Profemur Modular-Neck Hip Implant Recall Claims Being Investigated by Bernstein Liebhard LLP Following Class I Recall for Thousands of Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck Components

Bernstein Liebhard LLP.

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Bernstein Liebhard LLP

Oct 09, 2015, 02:57 ET

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NEW YORK, Oct. 9, 2015 /PRNewswire/ -- Bernstein Liebhard LLP is now investigating legal claims related to the recent MicroPort Profemur Modular-Neck Hip Implant recall for thousands of Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck components. China-based MicroPort Orthopedics, Inc. announced the voluntary recall in August, after the affected components were associated with an unexpected rate of fractures. On October 2nd, the U.S. Food & Drug Administration (FDA) deemed this action a Class I recall, which indicates that the affected components pose a serious risk of injury or death.

"Patients who have received Profemur modular necks are at risk for sudden, catastrophic fractures which have the potential to cause other serious health problems. Our Firm would like to hear from anyone who has undergone hip revision surgery due to complications that may be associated with the MicroPort Profemur Modular-Neck Hip Implant recall," says Sandy A. Liebhard LLP, a partner at Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The Firm is now offering free, no obligation legal reviews to individuals who were allegedly injured as a result of devices included in the Profemur Modular Neck recall.

MicroPort Profemur Modular-Neck Hip Implant Recall

The Profemur Long Cobalt Chrome 8 Degree Varus/Valgus Modular Neck components affected by this recall are part of MicroPort's Profemur Modular-Neck Hip Implant System. This system consists of interchangeable parts that allow a surgeon to fit the hip implant to each patient's unique anatomy.

According to the FDA, 10,825 Profemur Modular Neck components are being recalled in the U.S. The affected components were distributed from June 15, 2009 to July 31, 2015.  MicroPort has acknowledged receiving 28 reports of implant fractures related to the recalled part, representing a 0.286% rate of fracture. The FDA has advised patients fitted with these components to contact their doctors at once if they experience a sudden onset of severe pain in their post-operative hip, difficulty or inability walking, significant trauma to their hip or leg (e.g. falling), or a tingling sensation or loss of feeling in their leg. Acute fractures of the modular neck may require emergency revision surgery, as such an occurrence has the potential to cause neurovascular damage, hematoma, hemorrhage, and even death.

This is not the first time questions have been raised about the safety of Profemur hip implants. MicroPort began manufacturing the Profemur line in 2013, after it obtained the franchise as part of its acquisition of Wright Medical Group's OrthoRecon business. Prior to the acquisition, Wright Medical had been named a defendant in a number of Profemur hip lawsuits filed on behalf of individuals who allegedly suffered injuries related to the premature failure of Profemur hip replacements.

Recipients of the component involved in the MicroPort Profemur Modular-Neck Hip Implant recall may be entitled to compensation if they experienced any complications allegedly associated with fracture of the modular neck. To learn more about Bernstein Liebhard LLP's investigation, please visit the Firm's website. To arrange for a free, o-obligation legal review, please call 800-511-5092.

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. As a national law firm, Bernstein Liebhard LLP possesses all of the legal and financial resources required to successfully challenge billion dollar pharmaceutical and medical device companies. As a result, our attorneys and legal staff have been able to recover more than $3.5 billion on behalf of our clients. The Firm was named by The National Law Journal to the Plaintiffs' Hot List, recognizing the top plaintiffs firms in the country, for 12 consecutive years. Bernstein Liebhard LLP is the only firm in the country to be named to this prestigious list for a dozen consecutive years.

Bernstein Liebhard LLP
10 East 40th Street
New York, New York 10016
800-511-5092

ATTORNEY ADVERTISING. © 2015 Bernstein Liebhard LLP. The law firm responsible for this advertisement is Bernstein Liebhard LLP, 10 East 40th Street, New York, New York 10016, 800-511-5092. Prior results do not guarantee or predict a similar outcome with respect to any future matter.

Contact Information:
Sandy A. Liebhard, Esq.
Bernstein Liebhard LLP
info(at)consumerinjurylawyers(dot)com
http://www.rxinjuryhelp.com/
https://plus.google.com/115936073311125306742?rel=author

Logo - http://photos.prnewswire.com/prnh/20120202/MM47134LOGO

SOURCE Bernstein Liebhard LLP

Related Links

http://www.bernlieb.com

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