Articles Posted in Mass Torts

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Millions of women use chemical hair relaxers on a regular basis. In 2022, new scientific research revealed that chronic exposure to the chemicals in hair relaxer products can cause uterine and ovarian cancer. This new evidence prompted a wave of lawsuits against the manufacturers of hair relaxer products by women claiming that they developed cancer as a result of using these products.

These cases are moving forward. The MDL judge has scheduled the first bellwether trial for November 3, 2025, with a second trial to follow in February 2026. These trials are intended to help both sides gauge how juries might respond to the evidence and could influence settlement discussions…if there is not a global settlement before the first trial, as many, including our lawyers, suspect.

Our mass tort lawyers have been at the forefront of the hair relaxer cancer lawsuits from the very beginning. We are currently accepting hair relaxer cancer cases from women across the country.  Call our office today for a free consultation at 888-322-3010, or get a free online consultation.

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If your premature baby died or suffered serious injuries from necrotizing enterocolitis (NEC) after being fed with formula such as Enfamil or Similac, you may be able to file a product liability lawsuit and get financial compensation.

Infant formula made from cow milk has been linked to NEC, and there is evidence that the formula companies knew about this link but negligently failed to warn consumers and doctors about it.

About Necrotizing Enterocolitis (NEC)

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From the early 1950s to the later 1980s, the Marine Corps base at Camp Lejeune in North Carolina provided residents and employees with drinking water heavily contaminated with toxic chemicals.

Extensive scientific research has revealed that the poisoned water supply at Camp Lejeune had a devastating impact on the long-term health of base residents, who have suffered significantly higher rates of birth defects, cancer, and neurological conditions.

Our lawyers are not taking new clients in this litigation. This page aims to give you the latest update on the Camp Lejeune litigation and answer some of your key questions.

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The Bard PowerPort is an implanted port catheter device positioned just beneath the skin to facilitate easy attachment to a catheter for the intravenous administration of fluids or medications. Unfortunately, the Bard PowerPort possesses inherent design and manufacturing flaws, increasing its susceptibility to fracturing and shifting from its intended position. This defect has the potential to result in severe injuries, including internal vascular damage. 

Individuals who have suffered injuries due to a faulty Bard PowerPort device are pursuing product liability lawsuits against the manufacturer responsible for producing these implants. Our law firm is actively receiving cases from individuals who have had a Bard PowerPort catheter device implanted and subsequently experienced injuries resulting from fracture, migration, or other malfunctions of the implant. 

PowerPort Lawsuit News & Updates

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In the world of antibiotics, Bactrim (sulfamethoxazole-trimethoprim) stands as a powerful weapon against bacterial infections. It works great. This combination medication, composed of two active ingredients, has saved countless lives by combating a wide range of bacterial invaders.

However, beneath its lifesaving capabilities, Bactrim hides a potential complication – its role in contributing to yeast infections. In this comprehensive article, we delve into the mechanisms of Bactrim, the enigma of yeast infections (Candidiasis), and how the two intersect, shedding light on an often-overlooked aspect of antibiotic treatment.

Bactrim

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If you or a loved one experienced pain, discomfort, or complications after receiving a BioZorb implant following breast cancer surgery, you are not alone. Across the United States, patients are taking legal action to hold the manufacturer, Hologic, accountable for the harm caused by this device.

The BioZorb implant, manufactured by Hologic, Inc., is a class II medical device first cleared by the FDA in 2012 under the 510(k) process. It is an implantable radiographic marker composed of a bioabsorbable material (polylactic acid) and six titanium radiopaque clips, which are designed to mark soft tissue sites during radiation therapy following breast cancer surgery. The device is intended to provide a three-dimensional marker for more precise radiation targeting while gradually dissolving in the body over time.

BioZorb works. But it has also been linked to several complications, including prolonged pain, discomfort, infection, device migration, and non-absorption. Many patients have reported the formation of hardened masses, scar tissue, and additional injuries at the implant site. The device has also been associated with increased radiation exposure and adverse reactions requiring further surgeries for removal.

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PFAS (per- and polyfluoroalkyl substances), commonly referred to as “forever chemicals,” are highly toxic chemicals. We now know that PFAS have been contaminating the groundwater used by millions of families across the U.S. Exposure to PFAS in groundwater can cause cancer and other major health issues.

Anyone who has been seriously injured as a result of exposure to groundwater contaminated by PFAS may be able to file a civil lawsuit and get financial compensation. A growing number of these lawsuits are already being filed across the country. This page will look at the basic allegations in these water contamination lawsuits and their potential settlement value.

We are currently accepting new water contamination cases. If you developed cancer or other serious health conditions from water contaminated by PFAS, contact us today at 888-322-3010 or contact us online. 

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In 2021, the surgical implant manufacturer Exactech announced a recall of all its Optetrak® implant systems used in total knee replacement surgeries since 2004. The recall came after the company discovered that a problem with the product packaging was causing the polyethylene insert component in the Optetrak implants to degrade not function properly. This defect is causing the Optetrak knee implant systems to prematurely fail which ultimately requires patients to undergo additional revision surgery.

Individuals who had the Exactech Optetrak system implanted and suffered premature failure due to this defect can file a product liability lawsuit against Exactech and potentially recover financial compensation for their pain and medical bills. Our firm is currently accepting Optetrak implant failure cases from patients who suffered a premature failure to their knee replacement implant and had to undergo revision surgery.

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Recent research has identified a potential link between asbestos exposure and breast cancer, broadening the scope of illnesses associated with this dangerous substance. While asbestos is most commonly connected to mesothelioma and lung cancer, studies now suggest that its toxic fibers may also play a role in breast cancer development. These findings are particularly significant for women who have experienced occupational or environmental exposure to asbestos, highlighting the far-reaching health risks of this material.

How Asbestos Exposure Can Lead to Breast Cancer

Asbestos fibers, when inhaled or ingested, do not easily break down or leave the body. Instead, they can embed themselves in tissues and persist for decades, creating chronic inflammation and cellular damage.

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Depakote, a brand name of the anticonvulsant medication valproate, is commonly used to treat various medical conditions, including seizures, migraine headaches, and bipolar disorder. However, there is growing concern about the use of Depakote during pregnancy and the risk of autism and attention deficit hyperactivity disorder (ADHD) in children.

Recent studies suggest associations between the anti-epileptic drug Depakote and adverse health effects. One study found that it increased the death risk in post-stroke epilepsy patients. Another found an association between Depakote use during pregnancy and the Autism and ADHD risk in children. In addition, individuals have filed lawsuits in France against Sanofi, the European manufacturer of Depakote.

About Depakote 

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