Articles Posted in Product Liability

Recently, the United States Judicial Panel on Multidistrict Litigation centralized the Ozempic lawsuits, at least 55 of them, in Pennsylvania federal court. These lawsuits allege that defendants Novo Nordisk and Eli Lilly failed to warn people of severe side effects linked to the diabetes and weight loss drugs Ozempic and Mounjaro. The plaintiffs allege they were prescribed drugs to treat diabetes or assist in weight loss but weren’t warned about serious side effects like stomach paralysis and intestinal obstruction. If you were harmed by Ozempic or Mounjaro, call the seasoned Chicago-based product liability lawyers of Moll Law Group. Billions have been recovered in product liability cases with which we’ve been involved around the country.

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In its order, the JPML agreed it would send all the Ozempic and Mounjaro cases to United States District Judge Gene E.K. Pratter in the Eastern District of Pennsylvania where 13 of the cases were already pending. The JPML believes the drugs are similar enough that one MDL for the cases would make discovery and other proceedings more efficient; it will also avoid the risk of inconsistent rulings. Judge Pratter can issue rulings and make consistent decisions that apply to side effect cases related to the relevant diabetes and weight loss drugs.

The defendant pharmaceutical companies denied the allegations in court and moved to dismiss the lawsuits on the grounds that the drugs’ potential side effects are known to the public and that the labels on the drugs announce the side effects, thereby providing adequate warnings.

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The Philips DreamStation 2 CPAP machine, used both at home and in medical settings, is prescribed to provide positive airway pressure for treatment of obstructive sleep apnea. Recently, the United States Food and Drug Administration (FDA) has warned patients and health care providers to diligently attend to whether their Philips DreamStation 2 continuous positive airway pressure (CPAP) machines are overheating. The warning was issued after the FDA realized that reports about thermal issues like burns, smoke and fire were increasing in connection with these CPAP machines; the agency received 270 reports of problems between August 1, 2023–November 15, 2023. If you were burned, suffered smoke inhalation, or another injury due to a CPAP machine overheating, should call the trustworthy 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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As a patient or caregiver, you should be aware that the affected Dream Station 2 CPAP machines were shipped in order to replace recalled DreamStation 1 CPAP machines. The foam used in the machines does not appear to be causing the safety issue. Rather, in a developing situation, it appears that there is an electrical or mechanical malfunction within the machine that can cause it to overheat under specific circumstances.

Patients, caregivers, and healthcare providers have been asked to ensure that the manufacturer’s instructions in the user manual are carefully followed. Among these instructions are to let the CPAP machine’s heater plate and water tank cool for 15 minutes prior to tank removal to reduce the burn risk and to inspect and examine the CPAP for atypical smells or appearance changes. If the machine exhibits any altered smell, appearance or sounds, or starts performing differently, the CPAP should be unplugged and left unused. Patients should ask their primary care physician or sleep doctor for next steps. Reports should be made to the FDA about these issues. Meanwhile the FDA continues to investigate and to discuss the manufacturer about mitigation strategies.

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Recently, federal safety regulators asked consumers to stop buying and using magnetic toy ball sets for their children’s use. These magnetic balls have now been associated with hundreds of serious injuries as well as 7 fatalities, 5 of them within the U.S. When swallowed, these toys magnets may attract to each other, which can result in intestinal blockages, blood poisoning and perforations of critical organs. If your child was injured or killed by magnetic toy balls, you should call the seasoned Chicago-product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

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Six notices about the magnetic toy ball sets have been issued. Once swallowed, toy magnets may attract to one another and cause severe injuries. The Consumer Product Safety Commission (CPSC) has identified 6 children’s toys that don’t comply with safety regulations because they include magnets that are small enough to be consumed by a child. There were 2400 ER hospitalizations from 2017–2021 involving people who ingested toy magnets.

One of the companies implicated, Xpressgoods.com, has agreed to issue a recall of 728 units of a magnetic ball set manufactured in China. Customers have been advised to return them for a full refund or store credit. However, other manufacturers based in China and South Korea haven’t agreed to offer remedies to consumers. The toy magnetic balls in questions are Magic QQ 216-Piece Mixed Color Magnetic Ball Sets, Ming Tai Trade’s 216-piece 5mm Magnetic Ball Sets, Sunny House 125-Piece 5mm mixed Color Magnet Ball Sets, Allvre 216-Piece 5mm Magnetic Ball Sets, Carrara Magnetic Ball Sets sold by myKmarket.com.

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Tesla makes almost 50% of the electric passenger cars sold in the United States. Recently, however, Tesla recalled more than 2 million of its cars. Previously, to no avail, federal regulators had pressed Tesla to update its Autopilot system, which can accelerate, steer, and brake by itself, and to make sure the cars’ drivers are paying attention in spite of the automatic driving features. This recall was Tesla’s fourth in under two years, and it covers almost all of the electric vehicles the company has made in the country since 2012. If you were injured because of Tesla’s electric vehicles, you should call the trustworthy Chicago-based lawyers of Moll Law Group. Billions have been recovered in lawsuits around the country with which we’ve been involved.

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Tesla has been successful in selling and marketing its electric passenger cars but has seen its market share slip as competitors have started selling electric cars. The recall, instituted after a National Highway Traffic Safety Administration (NHTSA) investigation into Tesla’s driver-assistance system, Autopilot, further damages Tesla’s image. Autopilot is designed to control vehicles on their own while driving down highways, but owner manuals ask drivers to continue to keep their hands on the wheel and resume control of the car in the event something goes wrong.

The investigation started in 2021 after fatal accidents occurred in cars that included the driver assistance technology. The agency identified 11 incidents that had occurred in which the Tesla vehicles were on the road with Autosteering engaged. Over the course of its investigation, the NHTSA said, it reviewed 956 crashes in which Autopilot was engaged, and focused on 322 crashes that included situations in which Autopilot might have been engaged inadvertently. The company has issued wireless software updates to some vehicles, and others will receive these updates later. The updates will involve more noticeable visual alerts while using autosteer, which will be suspended if drivers repeatedly fail to use it in a responsible manner.

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Recently, manufacturer WanaBana agreed with the FDA to voluntarily recall all WanaBana apple cinnamon fruit puree pouches because they have elevated lead levels. The warning asked parents and caregivers of children who consumed the pouches to contact their healthcare providers to get blood tests and advised parents not to buy WanaBana apple cinnamon fruit puree pouches. If your child may have been harmed by these pouches, 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 injured consumers nationwide.

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The FDA became aware of an issue with the apple cinnamon fruit pouches after four children were discovered to have elevated blood lead levels. The North Carolina Department of Health and Human Services examined multiple lot codes of the pouches and found very high lead concentrations. The FDA looked over the state department’s analytical findings and determined they could cause acute toxicity. The agency told the manufacturer that the pouches were a potential source of lead exposure. For its part, the manufacturer agreed to a voluntary recall once the FDA’s investigation found that all lot codes and expiration dates were affected. The pouches are sold across the country and are made available at retailers including Dollar Tree, Amazon, and Sam’s Club.

The company told the public that it is dedicated to making sure its products are safe. It also told consumers to stop using the product. It’s important to retain the pouch, if you can, when your child has symptoms of lead exposure, in case it’s needed for a product liability lawsuit.

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The Joint Commission has released its data for the first half of 2023, and alarmingly, it shows that sentinel events are on track to surpass a record high found in 2022. Sentinel events are patient safety events that cause severe temporary harm, permanent harm, or death. If you or a loved one were injured through a doctor or staff error at a medical practice, please call the seasoned Chicago medical malpractice lawyers of Moll Law Group. We also handle claims regarding dangerous drugs and medical devices, making us ideally positioned to look at all angles by which liability may be proven.

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Sentinel events are very serious. Among the common causes of sentinel events were teamwork failures, communication failures, failure to adhere to standard policies and procedures, wrong site surgery, wrong procedure, wrong patient, assault, rape, sexual assault, suicide, and treatment delays that cause further harm.

The injuries that result from these events can change the lives of you and your family forever. According to the Joint Commission data for the first half of 2023, of 720 reported and reviewed events during this time period, 18% caused patient death, 63% cause severe temporary harm, and 7% caused permanent harm. Tragically, many of the events were completely preventable.

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Recently, a jury found the company Bayer liable in a product liability lawsuit brought by plaintiff Mike Dennis who alleged his non-Hodgkin lymphoma was the result of exposure to Bayer’s Roundup weed killer. The jury ordered Bayer to pay $332 million in damages, of which $7 million is in compensatory damages and $325 million is in punitive damages. If you developed cancer and believe it was caused by exposure to Bayer’s Roundup, call the experienced Chicago-based lawyers of Moll Law Group. We represent clients nationwide.

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The $332 million damages verdict was the third trial loss for Bayer this month. The prior verdicts in Roundup trials were $175 million and $1.25 million. However, these wins for the plaintiffs came after a string of nine consecutive trials with similar claims. In 2020, Bayer settled most of the Roundup claims against it for up to $10.9 billion. Around 40,000 Roundup-related cases are still in process against it.

With regard to this verdict, the jury agreed with Bayer in connection with two out of four legal claims. It found that the company failed to warn of Roundup’s risks, but that it was not negligent, and that the product was not defectively designed.

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