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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.

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A class action lawsuit has been filed against American Express Company and American Express Travel Related Services Company, Inc. The lawsuit accuses these companies of imposing anti-competitive practices in the credit card market.  The plaintiffs’ lawsuit is based on a combination of federal and state antitrust laws, state consumer protection statutes, and claims of unjust enrichment.

This week, a group of debit card users has achieved class certification in a lawsuit against American Express Co. The class, representing users from 11 states and the District of Columbia, alleges that American Express’s rules have indirectly inflated rival card costs.

What Is the American Express Lawsuit About?

The lawsuit, filed in the United States District Court for the Eastern District of New York, represents a collective action on behalf of millions of consumers and entities who have used electronic payment methods other than American Express cards. The plaintiffs allege that American Express’s Anti-Steering Rules in its merchant agreements have unreasonably restrained trade and inflated prices in the credit and charge card transaction market.

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Recent findings have revealed elevated levels of harmful heavy metals, including arsenic, lead, and mercury, in numerous prominent baby food brands. These toxic substances are known to induce neurological and other health issues in developing children. The ingestion of these hazardous baby foods is suspected to be associated with the onset of conditions such as ADHD and autism.

Our legal team specializing in toxic baby food cases is currently open to new claims from children who suffered injuries or negative effects due to the consumption of these unsafe baby foods. If your child was fed Gerber brand baby food or “Earth’s Best” brand baby food and subsequently diagnosed with Attention Deficit Disorder (ADD or ADHD), autism, or another form of neurological disorder, contact our product liability attorneys today. You may be eligible for financial compensation.

Heavy Metals Found in Baby Foods

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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. 

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Thousands of women have filed lawsuits alleging chemicals in their hair relaxer products caused them to develop cancer. On this page we will explain who qualifies to file a hair relaxer lawsuit. We will also look at the primary injuries being alleged by plaintiffs in the hair relaxer cases.

What are the Hair Relaxer Lawsuits About?

Recent scientific findings have unveiled a potential correlation between prolonged hair relaxer usage and elevated occurrences of uterine cancer. Uterine cancer, ranking as the fourth most prevalent cancer among women, sees around 65,000 new cases reported annually in the United States, representing about 3.5% of all cancer cases. Notably, the incidence of uterine cancer in Black women is twice as high as in White women in the country.

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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.

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Cheryl Caldwell has filed a class action lawsuit against Nordic Naturals, Inc., alleging deceptive labeling practices regarding their product “Ultimate® Omega 2X.”

Caldwell claims the “2X” designation misleads consumers into believing that the product contains twice the omega-3 content of Nordic Naturals’ “Ultimate® Omega” product. Contrary to this implication, “Ultimate Omega 2X” contains 2150 mg of omega-3 per serving, not the 2560 mg that would represent double the “Ultimate Omega” product’s 1280 mg. Caldwell argues that this discrepancy results in the product having 16% less omega-3 than what is suggested by the “2X” label.  Let’s all admit that 16% less is not “2X” but it is not that far off, right?  But still, I get it. Misleading is misleading.

Nordic Natural Class Action Claims and Allegations

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TRESemmé is a popular brand of shampoo and other hair care products made by Unilever, Inc. Recently, consumers have filed lawsuits alleging that TRESemmé shampoo contains harmful chemicals such as formaldehyde that have caused users to suffer hair loss.

About Unilever and TRESemmé

Unilever is a major manufacturer of personal care products and it is the second leading manufacturer of shampoo in the world. TRESemmé is one of Unilever’s most popular hair care brands. The TRESemmé Products are sold directly by Unilever through retailers.  Unilever promotes TRESemmé Products through labeling and advertising channels, including representations written or approved by Unilever on retail websites like Walmart.

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Ozempic (semaglutide) is a widely used prescription medication for type-2 diabetes and weight management. Recent scientific studies indicate that higher doses of Ozempic can lead to gallstones and gallbladder disease, often requiring surgical intervention for gallbladder removal. Research has also shown that Ozempic can cause gastroparesis, a a serious condition that causes food to move too slowly through the stomach to the small intestine.

Until recently, the warning label for Ozempic failed to inform patients and physicians about the risk of gallbladder-related issues or gastroparesis. Individuals who experienced gallbladder disease or gastroparesis after using Ozempic may have grounds for financial compensation through a product liability lawsuit. Lawsuits against the drug’s manufacturers emerged in 2023 and will soon be consolidated into an Ozempic class action lawsuit.

For those involved in an Ozempic-related gallbladder lawsuit, contact our attorneys today at 800-322-3010 or reach out online for a complimentary consultation.

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A new class action lawsuit has been filed in Illinois federal court against The Quaker Oats Co., alleging negligence in ensuring the safety and quality of its granola products. This negligence led to the recall of over 90 varieties of breakfast items and snacks, suspected of being contaminated with salmonella during production.

On December 15, the Chicago-based company announced the recall of certain granola and oat bars and cereals due to potential salmonella exposure during processing. Salmonella is known to cause serious illnesses. The recall includes Quaker Chewy Bars in various flavors, multiple Quaker Simply Granola Oats varieties, and several Quaker snack mixes, as stated by the U.S. Food & Drug Administration.

January 12, 2024 Update

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