Articles Posted in Product Liability

Many people use continuous positive air pressure (CPAP) machines because they have sleep apnea, a common condition. Symptoms of sleep apnea that CPAP machines are meant to address include excessive daytime sleepiness, heavy snoring, memory difficulties and fatigue. When sleep apnea isn’t treated, the result can be depression, diabetes, heart disease, or high blood pressure. However, in 2021, Philips Respironics, which makes CPAP and BiPAP machines, along with ventilators, issued a voluntary recall because the polyester-based polyurethane (PE-PUR) sound abatement foam used in some of its machines carry health risks. CPAP lawsuits are likely to arise over the course of the coming year, 2022. If you were harmed by a CPAP machine, or believe you may have been, you should call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

The devices affected by the recall were made between 2009 and 2021. The warning from CPAP machine manufacturer Philips Respironics indicates that the PE-PUR foam used in its machines can degrade and enter the air pathway of the device. A consumer could develop serious, even fatal injuries, from inhaling black debris and chemicals from this foam. Consumers have been encouraged to get their devices repaired or replaced. As of October 2021, the manufacturer had made around 750,000 repair kits and replacement devices. It expects that the process of replacing all the affected devices could take around 12 months. But what if you have already been harmed by your CPAP machine?

Give Us a Call If You Believe You Might Have a CPAP Claim

If you were injured by your CPAP, you may have viable grounds to bring a product liability lawsuit against Philips Respironics and you should give us a call to talk about your situation. Product liability lawsuits can be filed against manufacturers in connection with manufacturing, marketing, or design defects in their products when those defects harm consumers. Those with successful lawsuits may be able to recover compensation for their losses including medical bills, lost wages, loss of enjoyment of life, and pain and suffering.

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Product liability lawsuits continue to be filed against manufacturer Abbott Laboratories for failing to warn parents that their baby formula Similac may cause premature infants to suffer from necrotizing enterocolitis (NEC), which is a very serious gastrointestinal infection. A motion has been made to consolidate 33 NEC lawsuits against the manufacturer in Illinois. If you believe your premature baby developed NEC due to Abbott Laboratories’ Similac formula, you should call the Chicago-based product liability attorneys of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

Discuss Your Potential NEC Claim with Moll Law Group

When you feed your baby, you trust that what you’re providing is reasonably safe for him or her to consume. Unfortunately, recent studies show that formulas made from cow’s milk, such as Similac, are dangerous for premature infants. In premature infants, there is an increased risk of the baby developing an extremely dangerous infection of their bowels called necrotizing enterocolitis (NEC) as a result of consuming cow’s milk. When a baby develops this infection, the tissue in his or her intestines decays rapidly, eventually resulting in perforations in the tissue of the intestinal wall. Bacteria then has an opening to leak into the abdominal cavity and can rapidly grow into a widespread systemic infection and sepsis.

A premature baby can develop mild, moderate, or severe NEC as a result of Similac. While a mild case isn’t life-threatening, a severe case can have permanent, even fatal consequences when it’s not properly diagnosed and treated. There is scientific evidence that dates back to the 1990s that connects Similac and preemies, but the more recent evidence is considered conclusive, such that the American Academy of Pediatrics strongly warns parents and caregivers not to feed Similac to premature infants.

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Recently, another lawsuit was filed on behalf of a farm worker alleging neurological injuries related to his application of paraquat, an herbicide, to farmlands to desiccate crops prior to planting new ones. Like many other lawsuits related to the herbicide, his complaint alleges failure to warn, design defects, negligence, breach of warranties, and public nuisance. Like many other plaintiffs, his injuries are consistent with Parkinson’s disease. Litigation against manufacturers of Paraquat, such as Syngenta and Growmark, has been ongoing since 2017. In December, Case Management Order 12 was issued for multidistrict litigation in Illinois. If you believe you may have suffered neurological injuries due to Paraquat exposure, you may have a claim for damages. Call the experienced Chicago product liability lawyers of Moll Law Group to discuss your case. Billions have been recovered in lawsuits with which we’ve been involved.

Studies conducted on animals have found that paraquat can do damage to dopaminergic neurons in the brain. It is, in fact, the agent used by scientists to produce Parkinson’s symptoms in animals because it is so effective at creating neurological injuries. Lawsuits are underway in federal courts across the country.

Consult Our Chicago-Based Lawyers About Your Injuries Arising Out of Paraquat

In Illinois, discovery, or the process by which each side gains information about the other side’s arguments and evidence, is now underway in the paraquat multidistrict litigation. Case Management Order 12 specifies that limited fact discovery for certain cases must be complete by March 31, 2022. The limited fact discovery allowed includes written fact sheets, requested documents, and up to 3 depositions per plaintiff. The defendant manufacturers can take depositions of the plaintiff, or a family member of the plaintiff, the plaintiff’s treating doctor, and a fact witness who can attest to the paraquat exposure. In order to get discovery beyond these three depositions, the manufacturer and plaintiff must agree or get the court’s permission.

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You may have used prescription strength Zantac, a heartburn drug, to treat and stop stomach ulcers and address gastroesophageal reflux disease (GERD). It’s important to be aware, however, that Zantac has been linked to cancer and discontinued. On October 8^th, a federal judge presiding over the Zantac multidistrict litigation ruled that the brand manufacturers of Zantac — GlaxoSmithKline, Sanofi, Pfizer, and Boehringer Ingelheim — should face lawsuits by people formerly prescribed the drug. If you were harmed by Zantac, you should call the experienced Chicago product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved around the country.

The court denied requests by manufacturers that it dismiss a class action related to the drug’s marketing and severe health issues. Additionally, however, the court ruled to dismiss all generic manufacturer cases; only cases against brand manufacturers may continue.

Losses from Zantac Use

The Zantac multidistrict litigation was pursued by patients prescribed Zantac who developed cancer and sustained losses as a result. Lawsuits allege that the drug’s active ingredient is an unstable molecule and that the Zantac drug label did not properly warn the public that a risk of cancer existed.

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In the 1960s, Paraquat entered the market as an herbicide. It’s been used to kill weeds and grasses before planting, to control weeds in orchards, and to dry plants prior to harvest. It can be applied with hand-held sprayers, knapsack sprayers, and pressurized tanks drawn by tractors or trucks. Lawsuits allege that there may be a link between the herbicide Paraquat and Parkinson’s disease. In June 2021, all Paraquat lawsuits filed in federal court were consolidated by the United States Judicial Panel on Multidistrict Litigation (JPMDL) under the Honorable Nancy J. Rosenstengel in the District Court for the Southern District of Illinois. If you were injured by the herbicide Paraquat, you should discuss your situation with the experienced Chicago product liability lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

Around 300 Paraquat lawsuits are now pending in the multidistrict litigation (MDL). One of the recent complainants is an Illinois man who worked for Therma Gas and Northern Star Minerals for a long period of time and sprayed Paraquat on potato crops being grown on land owned by Northern Star Minerals. In the course of that time, the man was unaware that his many years of Paraquat exposure could give rise to serious health issues. His Parkinson’s disease symptoms began in 2008, but he only realized that Paraquat had been linked to Parkinson’s in or after the summer of 2021.

Paraquat and Parkinson’s Disease

Paraquat is sprayed on around 15 million crops around the country. It is highly toxic and categorized as a restricted use pesticide. Only certified applicators are allowed to use it. Officials have not approved it for use in backyards. Lab studies show that the herbicide has the potential to damage neurons in the brain that are responsible for Parkinson’s. In fact, it is a toxin that is used to create animal models for the disease.

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The 3M lawsuits arising out of defective earplugs worn by servicemembers have been consolidated into the largest multidistrict litigation (MDL) in history. The MDL is larger than the asbestos and talc product cases. In the litigation, United States military veterans and service members have alleged they experienced hearing damage because they used 3M’s Combat Arms earplugs, Version 2 (CAEv2). If you were harmed by defective earplugs, you should give the experienced Chicago-based lawyers of Moll Law Group a call. Billions have been recovered in cases with which we’ve been involved, and we represent clients around the country.

The earplugs at issue were used by many servicemembers deployed in Afghanistan and Iraq between 2001 – 2015. The leading cause of disability among veterans, according to the Department of Veterans’ Affairs is hearing damage. In 2018, 3M paid $9.1 million to settle the United States government’s claim that it concealed defects in the earplugs; however, it didn’t admit it was liable for damages. The multidistrict litigation is presided over by Judge M. Casey Rodgers.

Around 200,000 cases are pending against the manufacturer 3M. Certain lawsuits have been selected for bellwether test trials. In this process, plaintiffs and defendants alternate in selecting specific cases to serve as bellwether cases, with each side trying to put forward cases they respectively believe are strongly in their favor. However, certain cases are chosen for trial by the judge because they don’t overly favor either the plaintiffs or the defendant.

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On November 12, 2021, the United States Food and Drug Administration (FDA) updated its recall of specific Philips Respironics ventilators, CPAP machines, and BiPAP machines. The recall for certain machines occurred on June 14, 2021. They were found to carry health risks connected to polyester-based polyurethane sound abatement foam that was used in them. The foam can deteriorate, resulting in severe injuries, which can be life threatening and cause permanent disabilities when medical intervention is not provided. If you were harmed by one of the machines in question, you should call the experienced Chicago-based product liability lawyers of the Moll Law Group.

The FDA inspected the Philips Respironics’ manufacturing facility to decide what contributed to the foam concerns. The FDA’s inspections include evidence production and testing, systems intended to make sure the product meets quality standards, review of records, staff training, and operations.

In the course of an inspection, an FDA investigator did observe issues outlined in an inspection closeout report.

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Chicago parents should remain alert to the possibility of furniture tip-overs. Certain dressers are not safe or carry a great hazard of tip-overs. A child can be quickly and silently crushed beneath dressers. Parents or other caregivers may not hear their cries, or they may not even have time to cry before suffering fatal injuries. Recently the Nova Series 5-Drawer Chest, Model B1428-10 was recalled by Magnussen Home Furnishings, Inc. of Riverside. Like many other chests, the recalled ones are unstable when they aren’t anchored to the wall, which means they present tip-over and entrapment hazards that can lead to a child’s serious injuries or even death.

The recalled Nova Series chests of drawers don’t comply with performance requirements set forth by the voluntary industry standard ASTM F2057-19. They are 54-inch brown dressers with walnut veneers. They were made between August 2009 – August 2015. They measure 18 inches deep and 40 inches wide.

You can check your dresser for a label on the back in the top left-hand corner. This label should incorporate both the month and year of manufacture as well as the model number. The recalled units have date codes that represent August 2009 and August 2015: AG09 and AG15.