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traffic-7859033_640Recently, Ford recalled 500,000 of its vehicles because of a problem with the hose in the cars’ rear brake system that can cause two models of its cars to experience a rupture that results in leaked brake fluid. The two models of recalled cars are 2016-2018 Lincoln MKX midsize luxury SUVs and the 2015-2018 Edge SUVs. If you were injured in a crash with either of these models, give the seasoned Chicago-based product liability lawyers of Moll Law Group a call. Billions have been recovered in cases with which we’ve been involved.

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Ford has explained that when its flexible brake hose has a leak, a driver may find that there’s an increase in brake pedal travel and an increase in stopping distance, a condition that increases the odds of a crash. When brake fluid gets low, a red brake fluid warning indicator light illuminates. The remedy for the problem with the brake fluid is expected to be available only in April. This is one of several Ford recalls in August—the company attributes the increase in recalls to its commitment to protect consumers, including by doubling its safety and technical expert teams.

If you were injured in a crash that was caused by low brake fluid, you should consult attorneys about whether you have grounds to file a product liability lawsuit. These are lawsuits brought to recover economic and noneconomic damages arising out of injuries from a dangerous and defective product.

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self-care-6886590_640On July 16, DermaRite Industries, LLC put in place a voluntary recall of certain products because of the possibility of microbial contamination from Burkholderia cepacia (B. cepacia) complex. Recently, this recall was expanded to a wider range of products and lots. If you suffered an illness due to contamination of one of the affected DermaRite products, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases around the country with which we’ve been involved.

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Burkholderia cepacia complex can spread through contact with contaminated surfaces or exposure to it in the environment, as well as by person-to-person contact. Symptoms of an infection depend partly on how a person who acquires it is doing in terms of their initial health upon contact. Some people experience no symptoms while others develop pneumonia, fever, shortness of breath, increased sputum, coughing, chills, redness, swelling, and pain at an infection site.

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urban-6712756_640-e1757035392842A new danger has emerged in vape shops and at gas stations and corner stores. Health officials warn that a concentrated kratom byproduct called 7-OH is being produced and marketed in ways that appeal to kids, and can be bought easily, even though it is believed to have effects and impacts similar to those of opioids. The 7-OH products are available to consumers in a range of forms and packages such as candy, fruit-flavored gummies, ice cream cones, drink mixes and shots, and tablets. Officials worry these products may represent the next stage of the opioid crisis. The FDA has  taken steps to get 7-OH restricted. If you or your child was harmed by 7-OH, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in product liability lawsuits around the country with which we’ve been involved.

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On July 29, the United States Department of Health and Human Services (HHS) let consumers know that the U.S. Food and Drug Administration (FDA) is taking steps to try to stop the availability of 7-OH. There’s been a recommendation to restrict some of the products that contain 7-OH under the Controlled Substances Act, for instance. Further, the FDA has provided consumers with educational materials, health care providers with a letter, and a scientific assessment that indicates people can develop opioid addiction when they use 7-OH products repeatedly or over a long time. The FDA has also sent warning letters to various businesses for illegal marketing of products containing the addictive substance.

7-OH, which appeared in products starting around 2023, is also referred to as 7-hydroxymitragynine, 7-hydroxy, 7-OHMG, 7-HMG, and 7. It is one of two psychoactive components that occurs naturally in kratom, which is a plant whose leaves were sold for medicinal and recreational purposes throughout the 2000s. There are only small quantities of 7-OH in kratom, but the products that are sold in cape shops have significant quantities of 7-OH; it’s believed that synthetic steps are taken to change another psychoactive component of kratom, one that exists in greater quantities, into 7-OH.

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male-7090164_1280-e1756575641203According to a recent wrongful death lawsuit against OpenAI and its CEO Sam Altman, a sixteen-year-old, Adam Raine, died by suicide in April after talking about suicide to ChatGPT for months. His parents, who have brought the lawsuit allege that ChatGPT coached him on how to commit suicide and that Open AI knowingly put profit over the safety of users when it launched GPT-4o version of its AI chatbot last year. Open AI has said it will change the safeguards on ChatGPT for vulnerable people, particularly putting into place additional protections for young people under age 17. If your loved one was harmed or died as a result of OpenAI’s ChatGPT or another AI chatbot, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in product liability litigation with which we’ve been involved.

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Wrongful death lawsuits are civil actions filed by surviving family members of the decedent for the purpose of holding a responsible party accountable for the decedent’s death. It can be brought when the party is responsible due to negligent, reckless or intentional acts, with the goal of recovering compensation for losses arising from the death, such as medical and funeral expenses.

Adam Raine’s parents’ lawsuit says that OpenAI knew that the bot had an emotional attachment component that could cause harm, but that the company was more concerned about dominating the AI market than making sure its product was safe. When GPT-4 came on the market last year, its valuation went from $86 billion to $300 billion. OpenAI has claimed that ChatGPT has safeguards like giving out crisis hotline numbers and sending users to other real-world resources; in a more recent statement, it acknowledged that parts of the model’s safety training can degrade over long-term interactions.

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job-5382501_1280-e1754760475318The Trump Administration has proposed elimination of the Consumer Product Safety Commission (CPSC), a bipartisan independent agency created by Congress that handles numerous product safety questions. An elimination of the agency would take crucial data-driven safety rules that protect people around the country from dangerous and defective products and immediately leave those rules vulnerable to political aims. The CPSC’s own 2026 budget request to Congress was the vehicle for the proposal of both agency elimination and an alarming reduction in consumer safety funding and staffing. This budget request, as well as an earlier leak of Administration documents that revealed a plan to get rid of the CPSC, have been strongly condemned by the Consumer Federation of America and other groups. There is still recourse if you or a loved one was injured by a defective or dangerous product. You should consult the seasoned product liability lawyers of Moll Law Group to determine whether you have a viable claim. Billions have been recovered in lawsuits with which we’ve been involved.

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The CPSC budget request proposes that CPSC functions be transferred to the Department of Health and Human Services (HHS). Meanwhile, the HHS is also experiencing a dramatic reduction in both funding and workforce. There have been layoffs, grant cancellations, and disruptions to public health programs around the country. In its criticism of the budget request for elimination, the Consumer Federation stated that it was fantastical to think that a new assistant secretary position could effectively utilize HHS administrative and support functions in the face of HHS’s huge budget cuts. The budget request, it says, will impair the ability to discover, respond to, and ultimately stop dangerous products from entering homes.

There are also 121 consumer advocacy groups that have called on Congress to reject the plan to collapse CPSC into HHS on the grounds that moving the agency could delay and weaken oversight, including the taking of important safety actions around dangerous products. The groups have asked Congress to maintain CPSC’s independence in the interests of household safety, and they’ve also asked Congress to fully fund the original fiscal year 2026 budget request from CPSC rather than follow the transfer plan. With the funds from the original budget request, the CPSC could conduct detailed investigations of emerging dangers, inform the public more clearly about safety problems, modernize its outdated technologies, stop dangerous items at ports of entry, and improve enforcement of product safety laws.

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splashing-165192_640Recently, the popular alcoholic beverage maker High Noon had to recall certain alcoholic seltzer products that were incorrectly labeled as nonalcoholic Celsius energy drinks. The recalled Beach Variety 12 packs had been mislabeled as Celsius Astro Vibe Sparkling Blue Razz Edition cans. Drinking what’s in the can will result in accidental consumption alcohol, which could cause significant problems for the unsuspecting consumer. If you or a loved one were injured as a result of consuming an improperly labeled High Noon alcoholic beverage, call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in defective product lawsuits with which we’ve been involved.

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Mislabeled 12-packs were sent to stores in eight states between July 21-July 23. They went to distributors and retailers in Florida, New York, Ohio, Oklahoma, South Carolina, Virginia, and Wisconsin. They were sent only to distributors in Michigan and Oklahoma.

The recalled High Noon Beach Variety Packs, which are 12-packs of 12 fluid ounce cans, have the following lot codes on the exterior of the 12-pack box: L CCC 17JL25 14:00 to L CCC 17JL25 23:59 and L CCC 18JL25 00:00 to L CCC 18JL25 03:00. The recalled Celsius Astro Vibe Sparkling Blue Razz Edition, consisting of 12 fluid ounce cans, have the following lot codes on the bottom of the cans: L CCB 02JL25 2:55 to L CCB 02JL25 3:11.

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baby-7213274_640-e1754760040240Tegu’s Magnetic Floating Stackers are children’s wooden toys that have a base, six pieces of different colors that stack, two posts, and two figures. All of these connect with magnets. Recently, Tegu recalled the Magnetic Floating Stackers toys due to the risk that a child would ingest the magnet, risk of serious injury or death, and a violation of the mandatory standard for toy magnets. If your child was harmed after ingesting magnets from the Teju magnetic floating stackers, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

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The Tegu Magnetic Floating Stackers were recalled on July 31, 2025—the recall affects 25,850 units in the country. The reason that the toys violate the mandatory standard for this type of toy is because the high-powered magnets in them can get loose and break free from the toy, presenting a danger to children. The consumed magnets may attract each other within a child’s digestive system. The result may be twisting, blockage of the intestine, perforations, blood poisoning, and even death. So far, there have been 31 reports to Tegu of magnets detaching from the toy stacker.

The affected model numbers are STA-BGY-801T (Rainbow) and STA-BTP-806T (Big Top). These were sold for around $40 at toy, children’s stores, and specialty stores around the country, and also on Tegu.com and Amazon.com from August 2018-April 2025). Consumers have been asked to take the product from children and reach out to the manufacturer for instructions to receive a free replacement stacker toy. However, if your child was injured or killed due to ingesting magnets, you should keep any remaining pieces in case they’re needed as evidence.

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sandwich-4638226_640Recently, Fresh & Ready Foods, LLC voluntarily recalled certain ready-to-eat sandwiches and snacks that were sold in California, Washington, Arizona and Nevada due to potential Listeria monocytogenes contamination. These were sold under the brand names Fresh & Ready Foods, Fresh Take Crave Away, and City Point Market Fresh Food to Go and distributed between April 18, 2025-April 28, 2025, in various facilities, buildings and corporate offices. The contaminated food has use-by dates from April 22, 2025- May 19, 2025. If you were harmed by Listeria-contaminated food, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

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This issue was identified through environmental monitoring conducted by the FDA during a site inspection, which resulted in a positive finding for Listeria monocytogenes on a piece of equipment. Fresh & Ready Foods has taken immediate corrective actions including removing equipment to address this issue to ensure ongoing food safety and compliance with FDA guidance.

Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, a Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.

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cough-syrup-2557629_640Recently, the manufacturer Medtech Products Inc., a Prestige Consumer Healthcare Inc. company voluntarily recalled five lots of the popular, widely used Little Remedies Honey Cough Syrup for children because the bacteria Bacillus cereus (B. cereus) was discovered. B. cereus can cause two kinds of food-borne illnesses. Parents trust that medicines for children are safe. If your child was made sick by Little Remedies Cough Syrup, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved. We represent clients around the country.

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In one kind of food-borne illness caused by B. cereus, the person who got sick has symptoms of stomach cramps, vomiting, and diarrhea that commence 1-6 hours after consuming the contaminated food item. In the other kind of food-borne illness from B. cereus, the sick person suffers from diarrhea and cramps that typically start 8-16 hours after consuming contaminated food. Exposure to high levels of B. cereus can result in death, but most healthy people only experience short-term illness.

The Little Remedies Honey cough syrup at issue comes in 4 fluid ounce amber bottles. They’re sold with their lot codes appear on the label on the bottle and on the bottom of the crate they come in. The lots affected by B-cereus were distributed around the country through retailers and online from 12/14/2022 – 6/04/2025. The affected lots and their expiration dates are 0039 (11/25), 0545 (1/26), 0640 (2/26), 0450 (5/26), and 1198 (12/26). Other Little Remedies products haven’t been made part of the recall.

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hospice-4135835_640-e1752357257868In May of this year, the manufacturer Medtronic voluntarily recalled Newport HT70 and HT70 Plus ventilators, along with specific service parts related to those models. Consumers were asked to remove these devices from use and substitute an alternative ventilator for patients. In June, the FDA designated the voluntary recall as a Class I recall—the most serious type of recall as it means the product has a reasonable possibility of causing severe medical problems or death. If you were injured or a loved one died due to Newport ventilators, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases across the country with which we’ve been involved.

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Ventilators, as their name indicates, provide a patient with ventilation, helping him or her to breathe by themselves. When a patient can’t breathe on their own, the result may be lowered oxygen levels and heightened carbon dioxide in the patient’s body, which in turn can result in brain injury or death. One family of recalled ventilators, HT70, is meant to be used at home to provide continuous or intermittent positive pressure mechanical ventilatory support for people that need mechanical ventilation. They are also used in cases involving infant or pediatric patients in subacute care, a hospital, an emergency department, and for emergency response situations, specifically because this population is at heightened risk of death or injury due to unpredictable ventilator failures.

The company has advised that certain of its ventilators no longer be used in clinics. Customer complaints led to Medtronic finding two distinct capacitators that could and cause the ventilator to shut down while it was being used or the shutdown alert alarm not sounding properly. When a ventilator experiences one of these failures and adequate ventilation isn’t provided, the person using the ventilator might not be able to breathe by themselves.

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