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Articles Posted in Product Liability

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ramillu-bbq-825711-scaled-e1776008397667Several different models of Nexgrill grill brushes were recalled recently. It was found that the small metal wire bristles in those brushes could detach from the grill brush and attach to the grill or to food. This presents a danger of ingestion, and consequently, the danger that someone could suffer serious injuries, including ones that necessitate surgery. If you were injured as a result of Nexgrill grill brushes sticking to your 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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Nexgrill has become aware of a minimum of 68 reports and reviews that state that the grill brushes’ small wire bristles detached. There were five reports of people who swallowed the metal bristles and needed medical care to get the bristles removed from their throat or digestive tract.

The recalled grill brushes, which are between 18 and 21 inches long, and have the word “Nexgrill” on them, were sold at Home Depot and online at homedepot.com from 2015 through 2026 for $5 to $15. They have black plastic or wood handles.

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publicdomainpictures-baby-21998-scaled-e1776007626807Recently, AirClub convertible bassinets were recalled because of the risk of severe injury or death as a result of falls. The bassinets were found to violate the mandatory standard for bedside sleepers because the mechanism that attaches the bassinet to an adult’s bed leaves a space between the bedside sleeper and mattress. An infant could fall through that space. If your infant was injured as a result of an AirClub convertible bassinet, you should consult the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in lawsuits with which we’ve been involved.

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The AirClub convertible bassinets were sold online at Amazon from October 2023 to December 2025 for between $110 and $130. These bassinets convert into a bedside sleeper. They come in the colors of purple, beige, and light grey and have quilted padding. Around 110,400 bassinets were affected by the recall. The label at the bottom of the bassinets, underneath the mattress pad, will say Product Model QX-831. Meanwhile consumers have been asked to stop using the bassinets right away and to contact the manufacturer for a replacement attachment mechanism.  No injuries or deaths have been reported yet.

It may be appropriate to pursue compensation by filing a product liability lawsuit against the manufacturer. These are lawsuits that are brought when a product, such as a bassinet, is defective in terms of its design, manufacturing, or marketing. Typically, it’s crucial to retain a knowledgeable expert or group of experts who can opine on whether the product has one of these defects and whether that defect caused your baby’s injuries or death. Generally, design defects are found in every unit of a product; the bassinet might have a design defect if the gap exists in every bassinet of that model. Manufacturing defects, meanwhile, are defects that occur only in certain units of the product; the exist because there has been a deviation from the specifications or design. Marketing defective often involve a failure to warn of dangers.

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fairpharma-person-8320937-scaled-e1776007184759The United States Food and Drug Administration (FDA) has announced that it discovered cases of liver injury among patients taking Amgen’s drug for a group of rare autoimmune diseases. The FDA asked healthcare providers to stop using this treatment if there’s a suspicion of organ injury or damage. If you were injured as a result of taking the Amgen drug—Tavneos—you should consult the seasoned Chicago-based lawyers of Moll Law Group. We represent clients around the country, and billions have been recovered in cases with which we’ve were involved.

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In its announcement, the agency stated that it had identified 76 instances of drug-induced liver injury and among those, eight deaths. The evidence suggests that these injuries may be caused by Tavneos. Among the injuries were seven cases of vanishing bile duct syndrome, which is a rare condition that can lead to permanent liver damage.

Tavneos is a medical treatment approved to treat anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis, which is a group of rare autoimmune diseases that inflame small- to medium-sized blood vessels.

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leo_65-dresser-2901980-scaled-e1776006614853Recently, 4our Kiddies tip restraint kits, which include plastic tip restraints, were recalled because it was discovered that they could degrade or break. They present tip over and entrapment dangers that could cause serious injuries or even death to children or older people who were engaged with furniture secured to the wall with the restraints. If you or your child was injured as a result of a tip-over or entrapment caused by 4our Kiddies tip restraint kits, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

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The 4our Kiddies tip restraint kits, which has plastic tip restraints or furniture straps, were sold on Amazon.com from June 2019 through January 2026 for $6 to $21. They were recalled on March 26, 2026, because they may have a hidden defect.

The Consumer Product Safety Commission has become aware of a minimum of 150 cases where consumers reported that the plastic tip restraint kits broke. Three of these cases involved tip-over accidents.

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alexis-feet-70573_640-e1773531784153The Cartiva Synthetic Cartilage Implant (Cartiva SCI) is a hydrogel implant created to treat painful toe arthritis at the big toe’s base. Recently, plaintiffs in five lawsuits moved under 28 U.S.C. section 1407 to centralize litigation about Cartiva toe implants in the District of Maryland or the Northern District of Illinois. There are plaintiffs in nine potential tag-along lawsuits in seven districts, and some of them also supported centralization in the Northern District of Illinois. If you were harmed by Cartiva toe implants, you should give the seasoned Chicago- based medical device lawyers of Moll Law Group a call to determine whether you have a viable claim. Billions have been recovered in cases with which we’ve been involved around the country.

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Each of the plaintiffs was implanted with the Cartiva Synthetic Cartilage Implant. These implants, which are put in place during a minimally invasive 30-minute outpatient procedure, are supposed to provide a cushioning effect, and allow for the replacement of painful, damaged cartilage without fusion of the joint.

In their lawsuits, the plaintiffs alleged that the implant was defective and that, as a result, they suffered from persistent pain and limited range of motion after being implanted with them and then needed further surgery to remove the failed implants and fuse their arthritic joints. Their claims were for strict product liability, negligence, and breach of express and implied warranties.

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stocksnap-people-2585648-scaled-e1774738650677The FDA has reported that, based on medical device maker Abbott Laboratory’s company data, there have been 860 serious injuries connected to the recall of certain glucose monitoring sensors. Internal testing at the manufacturer determined that certain sensors can offer incorrect readings of low glucose. The consequences of this may involve injuries, complications, or even death. If you were harmed by one of the FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in cases around the nation with which we’ve been involved.

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In November 2025, Abbott issued a medical device correction, reporting that there had been 736 severe adverse events and deaths connected to certain affected glucose monitors. These events and deaths occurred on an international scale. When incorrect glucose readings go without detection, inappropriate treatment decisions for diabetic people may be made. For example, patients may consume excess carbohydrates or may skip or delay insulin doses.

Around 3 million Libre 3 and Libre 3 Plus sensors from a specific production line, around half of which were used or have expired were affected. The FDA issued an early alert in December. In January, the FDA classified it as a Class I recall, which is the most serious type of recall, on January 14, a company spokesperson told Reuters. Class I recalls occur when an affected product could cause serious injury or death if consumers continue to use it.

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ccipeggy-grocery-store-2619380_640-e1773530069664The Food and Drug Administration (FDA) has announced its goals for 2026 when working to promote the health of Americans with its Human Foods Program (HFP), which is a vital part of the implementation of the “Making America Healthy Again” program, advanced by the Trump Administration and the HHS Secretary Robert F. Kennedy. The federal government is focused on the crucial role of food and nutrition in health. If you were harmed by dangerous food or additives, you should call the Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in the cases with which we’ve been involved around the country.

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The FDA regulates around 80% of the country’s food supply. The HFP looks over all activities connected to nutrition and food safety with an eye toward making sure that food goes toward wellness and health of the American public. The program looks at chemicals in food, reduction of diet-related chronic disease and foodborne illness.

The HFP has multi-year initiatives to the end of promoting American Health through nutrition. Some of these initiatives are concerned with removing petroleum-based dyes from food, review a range of food additives and ban them if they’re unsafe, and comprehensively review infant formula nutrient requirements.

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grill-500547_640-e1769901385507A San Jose, California-based manufacturer of cookware items, IKM, is recalling certain pots and pans, because they might be contaminated with significant lead levels, which can get into consumers’ food. Lead is toxic and can impact people of any age or health; no level of exposure to lead is considered safe. If you believe you suffered lead poisoning due to IKM products, you should call the seasoned Chicago-based product liability attorneys of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

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The recalled items are the IKM aluminum saucepan wooden handle 9 inches (56 pieces); the A-cook Aluminum Kadai size 5 (43 pieces); the brass tope (10 pieces), and the IKM 4-quart Pital brass pot (9 pieces). No illnesses have been reported to date.

However, even low levels of lead exposure can result in significant health problems, especially in fetuses and children because of their rapid growth, metabolism, and smaller body size. When the levels of lead are lower, there may not be clear symptom, but the child may still struggle to learn and to suffer from low IQ and behavioral issues. When lead levels are high, the symptoms can include neurological changes, stomach pain, headache, and fatigue.

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baby-6823431_640-e1769900986959Recently, Nestlé expanded its recall of infant and follow-on formula, after concerns about a heat-resistant toxin, cereulide, emerged, to over 50 countries. Cereulide can cause food poisoning. While no illnesses have been reported in connection with recalled products, parents are still warned to look out for symptoms. The recall impacted a range of infant nutrition products. If you believe your infant became sick because of Nestlé infant formula, 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. We represent plaintiffs around the country.

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Infant formula and follow-on formula were initially recalled after Nestlé’s testing discovered, during routine self-monitoring, that part of the production line had suspected Bacillus cereus contamination. Additional testing occurred and they found that cereulide, which is a toxin produced by specific strains of Bacillus cereus, was found in one of the raw materials, arachidonic acid oil (ARA), along with oil mixes containing ARA, that were used to produce the formula.

These findings caused Nestlé to expand the recall’s scope to include more products and additional countries where the facilities may have used that ingredient.

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cleaning-bucket-1290940_640-e1769900771559Recently, Clorox agreed it would pay a $14.15 civil penalty for knowingly failing to immediately report a bacterial hazard—a defect that could create a substantial product hazard of generated an unreasonable danger of serious injury or death— with Pine-Sol Scented Multi-Surface Cleaning Products. If you suffered harm as a result of using certain Pine-Sol Scented Multi-Surface Cleaning Products, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. We represent plaintiffs around the country, and billions have been recovered in cases with which we’ve been involved.

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In 2019, Clorox microbiologists put out a written report documenting bacterial contamination in finished product and storage tanks, which they specified was “possibly a Pseudomonad.” After that, the company got reports that certain products in stores were cloudy. Similarly, a distributor notified the company of the same problem in multiple locations. While Clorox took steps to mitigate the potential for bacterial contamination, Clorox did not immediately report to the Commission as required.

CPSC suggested that the proposed settlement sent the message that firms that delayed in reporting serious risks would risk paying significant penalties.

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