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There  1,300 Zimmer NexGen knee product liability lawsuits are pending throughout the country.  Countless more victims are waiting on the sidelines (maybe soon to lose their rights because of the statute of limitations).

The progress on these knee replacement lawsuits in recent months can best be summarized by “well, they are coming along.”  Now, at least, there is a more concrete plan to move this litigation forward.

On March 24th, Judge Rebecca R. Pallmeyer, the judge overseeing all the consolidated federal cases pending in the U.S. District Courts, identified six cases that will be part of the “initial tranche” of Zimmer NexGen bellwether trials. A bellwether trial consists of test cases that allow the parties to see what a jury will do with a claim that is typical of the class.  Why?  So the parties can get a better idea of the value of the cases.   These are called bellwether cases, often precursors for settlement talks, are expected to begin in 2015.

First introduced in 1995, NexGen Complete Knee Solution System was one of Zimmer’s most successful knee products.

In 2001, Zimmer attempted to capitalize on the success of this product line by releasing a modified version of the original design, the NexGen Flex line of products, designed to achieve 155 degrees of flexion.

Most components were approved without extensive trials or FDA investigation into their safety through the 510K fast-track approval program.  This FDA program allows medical devices to enter the market without requiring manufacturers to conduct clinical studies.

Instead, the manufacturer must only demonstrate the device is substantially equivalent to other similar products already on the market. So the actual product that goes into a patient’s knee is not tested like these medical devices should be tested.

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Injectafter lawsuits have been filed around the country amid allegations that the iron supplement causes hypophosphatemia (HPP), leading to fatigue, muscle pain and weakness, and bone pain.

Infectafer Lawsuit Update – July 2022

A total of 13 Injectafer product liability lawsuits have been filed in federal courts so far in 2022. 12 of the 13 Injectafer lawsuits were filed in the Eastern District of Pennsylvania and 1 of the cases was filed in the Middle District of Florida.

In Charlton v. Troy, a Pennsylvania Superior Court nixed a $40 million verdict, ordering a new trial in a birth injury lawsuit alleging excessive traction caused a severe spinal injury.

Facts of Charlton v. Troy

The case revolves around the events that occurred during the birth of the Charlton twins. Mrs. Charlton underwent routine prenatal testing at the hospital when she was 37 and a half weeks pregnant with twins. The ultrasound revealed that “Twin B” was 25 percent smaller than “Twin A,” indicating discordant growth and some tachycardia in Twin B.

Cauda equina syndrome is a neurological disorder that stems from an injury to the nerve root bundle that exits the spinal cord.

Symptoms of CES include severe back pain, weakness or numbness in the legs, bowel or bladder dysfunction, and sexual dysfunction. If not treated promptly and adequately, CES can lead to permanent nerve damage and even paralysis.

When a patient presents with symptoms of cauda equina syndrome, healthcare professionals must recognize the condition promptly and provide appropriate treatment. Unfortunately, medical malpractice can occur when healthcare providers fail to diagnose or properly treat CES, leading to permanent nerve damage, paralysis, and other long-term injuries.

If you or a loved one has suffered from CES due to medical malpractice, you may be entitled to compensation for your injuries. Our experienced malpractice attorneys can help you understand your legal rights and pursue justice via a medical malpractice lawsuit on your behalf.

cauda equina settlements

The treatment for cauda equina syndrome is generally immediate surgical decompression. The sooner this can be achieved, the better. You usually have a 48-hour window of opportunity to reverse the symptoms. The malpractice lawsuits occur when the symptoms were there to be seen during that window but were missed, usually in the ER or by a primary care doctor, or by the surgical staff after spinal surgery.

Cauda Equina Syndrome Causes and Symptoms

CES is caused by compression of the cauda equina nerves located at the base of the spinal cord. The condition can result from a variety of underlying factors, including:

  • Herniated disc
  • Trauma to the spinal cord
  • Tumor or lesion on the spinal cord
  • Spinal stenosis
  • Infection or inflammation

Symptoms of cauda equina syndrome can include:

  • Severe back pain
  • Weakness or numbness in the legs
  • Loss of bladder or bowel control
  • Sexual dysfunction
  • Numbness in the groin or genital area
  • Loss of sensation in the buttocks, inner thighs, or back of the legs

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Over 60,000 women in the U.S. get diagnosed with uterine cancer every year, making cancer of the uterus the 2nd most common female cancer. Recently, uterine cancer has been linked to exposure to certain chemicals, putting this disease at the center of several mass torts, including hair relaxer lawsuits and Camp Lejeune toxic water lawsuits. On this page we provide a simple overview of uterine cancer from a medical standpoint and look at how it has become involved in litigation.

The Uterus

The uterus is the largest female reproductive organ. This pear-shaped organ is often called the “womb” and is where human life begins in the form of fetal development during pregnancy. The uterus is comprised of 3 separate parts: (1) fundus, (2) isthmus, and (3) cervix.

Last week, the FDA announced Abbott’s recall of its Dragonfly OpStar Imaging Catheter on May 26, 2022. Abbott recalled the device because some parts of it may break off and remain in the body. The FDA reported that this defect may cause severe injuries, including ischemia, infections, embolisms, thrombosis, and death.

What is a catheter?

 A catheter is a flexible tube that healthcare providers insert into a narrow opening in the body. They are used in various medical procedures, including:

Cowboys star wide receiver CeeDee Lamb was sued last week by a sports memorabilia and trading card company after Lamb allegedly breach a contract with the company by failing to autograph a certain number of player cards.

The lawsuit drew some attention because sports memorabilia companies rarely sued players for this sort of thing.

Literally, since I started writing this piece,  the lawsuit became moot. Yesterday afternoon the memorabilia company announced on Twitter that Lamb had fulfilled his obligations under the contract.   Because often filing a lawsuit is what is needed to wake someone up who is not fulfilling their obligations.  But I finished the post because it is a good story.

Reglan is a pharmaceutical drug used to combat heartburn and slow gastric emptying in diabetes patients. The question is whether tardive dyskinesia (also known as TD), a neurological disorder with symptoms including repeated involuntary movements, is connected to Reglan use.

Below is a question and answer for about the Reglan lawsuits. This will read a little odd in places because much of it was written thirteen years ago. But it has 2022 additions as well, including a discussion of the possibility of a new Reglan lawsuit over the undisclosed stroke risk.

What Is Reglan?

Last week, the 2nd bellwether test trial in the C.R. Bard hernia mesh MDL ended in a verdict for the plaintiffs awarding total damages of $255,000. This verdict marked a solid victory for the hernia mesh plaintiffs and helped reaffirm the course of the litigation after the 1st bellwether trial resulted in a defense verdict last month. There are still over 16,000 additional plaintiffs with hernia mesh lawsuits pending in the MDL. Two additional cases had previously been selected for bellwether trials but the schedule moving forward is very uncertain.

Background on the C.R. Bard Hernia Mesh Lawsuits

C.R. Bard (now a subsidiary of Beckton-Dickinson) was one of the leading manufacturers of hernia mesh patches and screens. A hernia mesh is essentially a very small synthetic screen material that doctors implant inside the body during hernia repair surgery. The screen helps to strengthen and reinforce the surgically repaired tissue.

In March 2022, Pfizer announced that it was recalling a popular blood pressure medication (Accuretic) after several lots of the drug were found to contain unsafe levels of a known carcinogen called nitrosamine.

At least for now, the recall appears to be related to isolated batches of the drug and Pfizer claims that it has no evidence of “adverse events” related to the contamination. There is still the possibility, however, that this could turn into a much wider problem and lead to a wave of product liability litigation.

In this post, we will review the details of the recall and assess the likelihood of any mass tort litigation (and we have a new 2023 update at the bottom).

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