Zimmer Knee Cases
MT Services LLC provides up-to-date lawsuit news on the Zimmer Knee cases and resulting multidistrict litigation as well as various services to assist victims with getting the help they need during this difficult time. These services include: Lawsuit Pre-Settlement Funding Cash Advances, Surgical or Medical Procedure Funding (or cash needs related to surgery), and Attorney Referrals to nationally recognized Zimmer Knee lawyers and law firms.
Zimmer Persona Knee Cases/FDA Class II Recall
The FDA announced a Class II recall for Zimmer’s Persona Trabecular Metal Tibial Plate knee implant. The recall affects all lots and sizes of the knee implant, affecting all 11,658 devices that were recalled, according to the FDA’s website. 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.
Possible Side Effects
Radiolucent lines – “large gaps in between knee replacement components or between the components and the bone” – can lead to a several different problems such as:
- Joint fluid
- Tissue damage
- Severe pain
- Bone damage
FDA Issues Recalls to Zimmer Inc. NextGen Knee
In 2010, the U.S. Food & Drug Administration issued a Class II recall to Zimmer Inc. over the NexGen Complete Knee Solution MIS Tibial Components, Locking Screw and Stem Extensions, affecting 68,383 devices that had already been implanted. Recalls were issued for various components of the NexGen knee mechanisms (the NexGen LPS femoral component, the NexGen LPS Flex gender femoral component, and the NexGen MIS tibial components).
An FDA Class II recall typically indicates that a device may cause “temporary or medically reversible” health problems, as well as a remote possibility of serious health problems.
In addition to the FDA Class II recall, a voluntary recall was made by Zimmer Inc., regarding the NexGen MIS Tibial Component, because according to drug watch, “one of the pieces could loosen or fail because of shoddy manufacturing.” The voluntary recall that was initiated affects 41,180 devices and includes eight sizes (1-8).
Zimmer Recalls affect over 100K devices
According to MT Services, the recalls that were made on various devices affect over 100K devices. The NexGen Flex devices have been implanted in approximately 150K patients, and today, there are over 1,000 lawsuits filed against Zimmer Inc. in state and federal courts throughout the U.S. The initial trial date is set for February 2015.
Federal lawsuits have been consolidated into multidistrict litigation (MDL) in the U.S. District Court in the North District of Illinois, with the first bellwether trial set to begin in 2015.
The devices were meant to increase range of motion and imitate natural knee function, but plaintiffs who have filed cases against Zimmer Inc. claim that the devices actually caused a range of complications.
Some of the injuries include:
- Decreased range of motion
- Extreme pain
- Tissue and/or nerve damage
- Bone degradation or fractures
- Blood clots
- Ultimate failure of device implant
First Zimmer NexGen Knee Bellwether Trial Approaching
The first bellwether trial in the multidistrict litigation (MDL) over the Zimmer NexGen Knee implant lawsuits has been scheduled to begin October 13th, 2015. There are currently more than a thousand cases against Zimmer Inc. which have been consolidated before a federal judge in Illinois (In Re: Zimmer NexGen Knee Implant Products Liability Litigation, MDL No. 2272).
If you, or a loved one, believe that you have suffered any injuries from a Zimmer Knee implant and need to speak with a nationally recognized Zimmer Knee law firm, fill out the application on the upper right hand part of this page or call MT Services’ toll free hotline at: 877.571.0405 where live agents can assist you with any lawsuit services that you may need.
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