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A National Personal Injury Law Firm > Zimmer Persona Knee Replacements Causing Harm

Zimmer Persona Knee Replacements Causing Harm

National Medical Device Attorneys | Helping clients with their Zimmer Persona Knee Lawsuits

The Zimmer’s Persona Knee replacement has had recalls and issues after reports of the implant becoming loose, causing pain and further medical complications.

Barely three years after it was approved by the Food and Drug Administration (FDA) in 2012, the Persona Knee replacement, made by Indiana-based Zimmer Inc., had to issue a Class 2 recall after reports of gaps between the implant and the bone and loosening of the medical device from the intended position.

This device is indicated for patients with severe knee pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis and polyarthritis, among other ailments.

The FDA issues a Class II Recall when a product may cause temporary or medically reversible adverse health consequences.

At Greg Jones Law we want to hold Zimmer responsible. Contact Greg Jones Law today for a free, no obligation consultation.

ZIMMER KNEE COMPONENTS MAY BECOME LOOSE

When Zimmer issued the recall of these devices, in the Spring of 2012, the cause was the metal tibial plate where becoming loose. This plate sits on top of the tibia, the bone that is supposed to join with this plate to make it secure. But the pain and instability caused by the loosening of the device made many patients to go back to surgery to take out the original implant and replace it.

The manufacturer’s reason for the recall was “an increase in complaints of loosening and radiolucent lines”.

Radiolucent lines are called of large gaps in between knee replacement components or between the components and the bone, which can cause a series of problems. Among others; joint fluid, tissue and implant-wear debris may lodge in the cracks, leading to bone damage called osteolysis, which is an early indicator of implant failure.

Any kind of loose implants can cause severe pain, swelling and tissue and bone damage.

Patients with the Zimmer Persona Knees who are affected by these problems may have the following symptoms associated with a knee implant failure:

Loss of mobility

Inflammation

Knee tightness

Knee instability

Persistent pain

If you have experienced suffering due to your Exactech Optetrak Knee Replacement. Contact us today at 855-566-3752 to speak with an experienced medical device attorney about your Exactech Optetrak Knee Replacement Lawsuit.

After the first recall, the Zimmer Persona Tibial Articular Surface Provisional (TASP) Shim tool used in the Zimmer Persona Knee surgery was also subject to a voluntary recall notification on February 4, 2014. On December 11, 2014, and “urgent medical device correction” was also issued that provided that the TASP shim tool must be manually cleaned and inspected for a new product insert. And on March 12, 2015, another manufacturer recall, for the same reasons, of the Persona Trabecular Metal Tibial Plate.

ADDITIONAL INJURIES DUE TO KNEE FAILURE

About a quarter of those affected by this defective knee replacement part that had to undergo surgery all over again to replace the implant had to face additional hospital stay, medical costs, time off from work, and time away from friends and family. That doesn’t include the additional pain and suffering, rehab and time taken from your family.

There are also further complications that may arise, like:

Pain and swelling

Nerve, tissue, or blood vessel damage

Bone loss

Infection

Risk of blood clots

Fractures and leg length discrepancies

Even after the revision surgery, many patients were unable to get permanent relief from their pain and had to continue living with it.

No patient should have to go through all this pain and suffering and be concerned about bills and being able to work to pay the bills and take care of their loved ones. Too often medical device manufacturers put making profit over people.

YOU COULD GET COMPENSATED FOR YOUR PAIN AND SUFFERING

Zimmer has a duty to provide safe products. Unfortunately, the manufacturer doesn’t have to live with the consequences of failing to warn of risks they knew or should have known of their product. Consequences that the victims and their families do have to live with every single day.

If there are risks of harm associated with their products, they also must provide adequate warnings to avoid fails like these or should be held responsible for the injuries they cause.

At Greg Jones Law we want to hold Zimmer responsible, to get you paid for you medical expenses, lost wages, pain and suffering and for any permanent disability you or a loved one may suffer.

We have a proven track record of helping victims of dangerous drugs and medical devices. Contact Greg Jones Law today for a free, no obligation consultation.

There is no money needed upfront and there’s no legal fees unless you get paid. In other words, if you don’t get paid, we don’t get paid.

Put an experienced knee replacement lawyer on your side. Contact us today!

zimmer persona knee failure

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