Articles Posted in Mass Torts

Published on:

By

From the early 1950s to the late 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 provides the latest updates on the Camp Lejeune litigation and addresses some of your key questions as this litigation drags on.

Continue Reading
Published on:

By

Millions of women use chemical hair relaxers on a regular basis. New scientific research three years ago 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 2early 2027.  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.

If you are looking for the most recent updates on hair relaxer lawsuits in 2025, we continue to provide timely information on case progress, bellwether trials, and potential compensation payouts for hair relaxer lawsuits. Our team remains committed to keeping victims informed as this litigation unfolds.

Continue Reading
Published on:

By

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

Continue Reading
Published on:

By

Numerous women have brought lawsuits concerning vaginal mesh against multiple medical device firms due to injuries stemming from flawed transvaginal mesh implants.

This article aims to outline the issues linked with vaginal mesh implants and their role in precipitating one of the most substantial mass litigation cases in history.

Additionally, it will provide updates on the ongoing vaginal mesh class action lawsuit and answer your questions about potential eligibility for individuals considering initiating their own legal action concerning vaginal mesh complications and what that will entail.

Continue Reading
Published on:

By

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 of their knee replacement implant and had to undergo revision surgery.

Continue Reading

Published on:

By

For several years, courts across the nation have been inundated with thousands of pending hernia mesh lawsuits. These product liability claims assert that hernia mesh implants from various manufacturers were defective, causing diverse complications post-surgery.

The lawsuits encompass multiple hernia mesh products produced by four medical device companies: Ethicon (a subsidiary of Johnson & Johnson that has recently settled most of its lawsuits), C.R. Bard (now part of Beckton Dickinson), Covidien, and Atrium Medical Corp. Lawsuits against each defendant have been consolidated into distinct class action MDLs.

Hernia Mesh Lawsuit Updates

Continue Reading
Published on:

By

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

Continue Reading
Published on:

By

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)

Continue Reading
Published on:

By
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.

Continue Reading
Published on:

By

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. 

Continue Reading