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On this page, we will look at who qualifies to file a Suboxone tooth decay lawsuit. We will summarize the basic eligibility criteria that our firm is applying to screen potential Suboxone lawsuits, and we will describe the relevant injuries associated with the Suboxone lawsuits.

About the Suboxone Lawsuits

Suboxone is a prescription drug that is commonly used for the treatment of opioid addiction recovery. There is overwhelming evidence showing that Suboxone causes chronic dry mouth which can lead to acute tooth decay and tooth loss. The manufacturers of Suboxone were aware of this side effect for more than a decade but failed to include any warning about tooth decay on the drug product label.

If you’ve undergone Tepezza treatment for an eye condition and experienced subsequent hearing issues like hearing loss or ringing in the ears (tinnitus), you might have grounds for a lawsuit and get financial compensation. Tepezza, a recently approved drug for thyroid eye disease treatment, has been shown to cause permanent hearing loss in some patients.

Those who received Tepezza and suffered hearing damage are now pursuing product liability lawsuits. Our legal team is actively pursuing cases related to Tepezza-induced hearing impairment across all 50 states. Reach out to us today at 800-322-3010 to determine if your situation qualifies.

UPDATES:

Lawsuits are being filed across the U.S. claiming that cow-milk based baby formula has caused many premature infants to develop a serious gastrointestinal infection called necrotizing enterocolitis (NEC). The basis for these lawsuits is that research has long shown that cow milk is associated with NEC in premature infants, and the manufacturers of formulas such as Similac and Enfamil should have warned doctors and parents of the risks. Our firm is currently seeking NEC formula lawsuits.  Plaintiffs who bring successful baby formula NEC lawsuit could receive significant financial compensation. 

Formula Can Cause Increased Risk of NEC in Premature Infants 

Infant formula products such as Similac or Enfamil are made from cow milk and given to newborn babies as a substitute for human breast milk.  A growing body of scientific evidence has proven cow milk formulas significantly increase the risk of a life-threatening bowel infection called necrotizing enterocolitis (NEC) when given to premature infants. 

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. 

About the PowerPort 

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 offer insights into potential eligibility for individuals considering initiating their own legal action concerning vaginal mesh complications.

About Vaginal Mesh Implants

Vaginal mesh, also known as transvaginal mesh, represents a specific type of surgical mesh implant utilized to reinforce and bolster weakened or injured tissue during surgical procedures. These mesh products are tailored for female pelvic reconstructive surgeries, commonly performed to address pelvic organ prolapse and/or stress urinary incontinence. These conditions arise due to the weakening of pelvic muscles, allowing organs such as the uterus, bladder, or rectum to descend into the vaginal area. Surgical intervention aims to repair and fortify these weakened pelvic muscles.

Between 1957 and 1987, the water supply at Camp Lejeune, a Marine Corps base in North Carolina, was contaminated with harmful chemicals at exceedingly high levels. Studies have demonstrated that exposure to this contaminated water while residing or working at Camp Lejeune led to the development of cancer, birth defects, and various health issues for numerous individuals. Unfortunately, North Carolina law has prevented these Camp Lejeune victims from pursuing legal action. However, the U.S. Senate is on the verge of passing a new federal law that will allow victims of water contamination at Camp Lejeune to file claims and receive financial compensation.

Our nationwide team of mass tort attorneys is now open to taking on new cases related to Camp Lejeune water contamination. We are specifically seeking victims who resided or worked at the base between 1957 and 1987 and subsequently received diagnoses such as leukemia, bladder cancer, kidney cancer, liver cancer, non-Hodgkin’s lymphoma, multiple myeloma, anemia, or other myelodysplastic syndromes.

Toxic Water at Camp Lejeune Base

In October 2023, the U.S. Food and Drug Administration (FDA) issued a significant recall of WanaBana fruit pouches due to elevated lead levels found in specific samples of WanaBana Apple Cinnamon Fruit Purée pouches. All WanaBana Apple Cinnamon Fruit Purée pouches, regardless of their expiration date, are included in this recall.

Following this discovery, the FDA urgently advised parents and caregivers to immediately stop providing these pouches to children and to safely dispose of any remaining products. Additionally, the FDA strongly recommended that toddlers and young children who might have consumed the recalled pouches undergo a blood test to check for potential lead exposure and consult with a healthcare provider.

Lead poisoning poses severe health risks, including developmental delays, learning disabilities, behavioral problems, and even fatal outcomes. Lead, a toxic metal, can harm the nervous system, particularly in children.