Articles Posted in Mass Torts

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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 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. Continue Reading

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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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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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A new study published in the Journal of Investigative Dermatology has raised alarms about the safety of popular acne products, many of which have been found to contain high levels of benzene, a known carcinogen. The findings highlight a significant health risk associated with these products, particularly as they are frequently used by teenagers and young adults. This is the second major analysis to reveal the presence of benzene in acne creams and cleansers, and it confirms concerns initially brought up by researchers earlier this year.

The Study and its Findings

Researchers tested over 100 benzoyl peroxide (BPO) acne products sold in major retailers across six states, uncovering that about one-third of these products were contaminated with benzene. Notably, products like Proactiv and CVS-brand face wash were found to contain benzene levels that far exceed the safety limits set by the FDA. Proactiv was found to have 18 times—18 times!— the amount of benzene allowed in U.S. drugs, while a CVS-brand face wash had 13 times the acceptable level. Such findings have led to increased calls for regulatory action and lawsuits to address this potential public health hazard.

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This page is about Veozah lawsuits for victims who have suffered a liver injury.

Veozah, a medication commonly used by women to alleviate hot flashes during menopause, has recently been linked to reports of serious liver injuries. Many women have turned to Veozah. It is, everyone seems to agree, an effective solution for many managing the uncomfortable symptoms of menopause, such as sudden sweating, intense heat, and rapid heartbeat that disrupt daily life. Yet, despite its effectiveness in reducing these symptoms, emerging evidence suggests that Veozah may pose a risk to liver health, leading to potentially severe complications.

Understanding Veozah and Its Use

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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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The Fosamax lawsuit suffered a long and slow death.  The plaintiffs did not deserve this long and awful ride.  But the litigation over a decade later appears to be (nearly) dead. This post was first written in 2013 and has been updated in 2023 and 2024.

September 2024 Foxamax Lawsuit Update

In a ruling that revives these lawsuits, the Third Circuit ruled that the FDA letter denying Merck’s proposed labeling changes for its osteoporosis drug, Fosamax, does not amount to a final agency action that preempts state law “failure to warn” claims. The decision centers on over 500 plaintiffs who allege that Merck failed to provide adequate warnings about the risk of atypical femoral fractures associated with the drug. The court concluded that the New Jersey federal judge wrongly prioritized FDA informal communications over the plaintiffs’ arguments against preemption.

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Snapchat, the popular social media platform operated by Snap Inc., has faced a series of Snapchat lawsuits in recent years alleging that its design features and inadequate safety measures have made it a breeding ground for “sextortion” and other forms of extortion and exploitation, particularly targeting minors. These legal actions have highlighted significant concerns parents have about this app’s responsibility to protect its young users from predators who misuse its features. The consequences when this happens can be tragic.

Snapchat

Snapchat, launched in 2011, quickly gained popularity, especially among younger demographics, for its unique features, such as disappearing messages, which kids love for obvious reasons, and multimedia sharing.