Lawsuitsettlementnews.com Reports FDA Class II Recall: Zimmer Persona Trabecular Metal Tibial Plate

Lawsuit website help center says that the U.S. FDA issued the notice for the Class II Recall on March 12th for Zimmer’s Persona Trabecular Metal Tibial Plate, affecting all lots and sizes of the knee implant.
By: MT Services LLC
 
BRONX, N.Y. - April 30, 2015 - PRLog -- MT Services LLC, a Lawsuit Settlement News Reporting Company which operates lawsuitsettlementnews.com, reports that the FDA announced a Class II recall for Zimmer’s Persona Trabecular Metal Tibial Plate knee implant. According to the FDA website, the recall affects all lots and sizes of the knee implant, affecting all 11,658 devices that were recalled. Also, according to an announcement made by the FDA, they said Zimmer Inc. initiated a voluntary recall of their Persona Trabecular Metal Tibial after there was an increase in complaints of loosening and radiolucent lines. All sizes and lots of the affected devices will be removed from the market and will no longer be distributed. A Class II Recall occurs when a product can "cause temporary or medically reversible adverse health consequences." Patients who have been implanted with the Persona Trabecular Metal Tibial Plate face the risk of their tibial component loosening. Indications of this complication include radiolucent lines on imaging tests, and such loosening may cause pain and issues with mobility, often requiring the patient to have an additional surgery.

Prior to this latest Class II Recall, Zimmer Inc. issued voluntary recalls for its metal-on-metal hip device – the Durom Cup, in 2008 – and another recall for the NexGen MIS Tibial Components in 2010. Those recalls led to lawsuits which are pending in a federal multidistrict litigation (In Re: Zimmer Durom Hip Cup Products Liability Litigation, MDL No. 2158) and Illinois (In Re: Zimmer NexGen Knee Implant Products Liability Litigation, MDL No. 2272).

Chris Janish, CEO of MTS, commented on the recent Zimmer Class II Recall, “We aren't surprised to see another voluntary recall on another Zimmer knee product. The current product has only had approximately 11,000 implants in the U.S., however, reports from our knee recall attorneys close to the litigation are that this product has an extremely high failure rate and could be the subject of thousands of filed lawsuit claims.”

MTS is ready and able to assist those who need lawsuit help and assistance obtaining a Zimmer knee law firm or Zimmer knee lawyer to provide a free evaluation on their specific case. To learn more about MTS’ services involving Zimmer Inc. as well as other defective product litigations, please visit: http://www.lawsuitsettlementnews.com/zimmer-nexgen-knee-lawsuit-news

If you already have an attorney on a filed a lawsuit involving a knee replacement that was previously recalled and need a lawsuit funding cash advance or lawsuit money, not to be confused with a lawsuit loan or pre-settlement loan, Lawsuit Settlement News can assist you with obtaining cash now as you wait for your settlement. Patients who have been affected from a Zimmer knee implant complication can apply for up to $25K in pre-settlement or settlement lawsuit funding. For a full list of the services that the company provides, visit: http://www.lawsuitsettlementnews.com/about-our-products-and-services

If you, or a loved one, have suffered complications from a Zimmer knee implant and need lawsuit money or lawsuit help, including finding a Zimmer knee attorney or Zimmer knee law firm, call 877.571.0405 to speak with an available agent. You may also fill out a quick application online at: www.lawsuitsettlementnews.com and an agent will contact you shortly.

Disclaimer:  MT Services LLC, operator of Lawsuitsettlementnews.com, is not a law firm and cannot provide legal advice on your case; however, MTS works with lawyers involved in mass tort litigations who are willing to provide a free legal consultation at the consumer’s request. For a list of full disclosures please visit the company’s website disclosure page.

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