Illinois Injury and Mass Tort Lawyer Blog

Published on: February 4, 2025

Seasoned Attorneys for Abbott Trifecta Valve Lawsuits

surgery-1807541_640-e1737155771843 In February 2023, Abbott, which manufactures Trifecta Valves warned doctors and other providers that its valves were subject to early structural valve deterioration. In summer 2023, the company announced that it would stop sales of the Trifecta Valves, including Trifecta Valve with Glide Technology (Trifecta Valva GT). Meanwhile the Food and Drug Administration (FDA) has offered many recommendations and continues to work with the manufacturer to determine the risks and best practices in connection with the affected valves. If you were injured or a loved one’s death is because of an Abbott Trifecta Valve that deteriorated early after being implanted, call the seasoned Chicago-based attorneys of Moll Law Group. Our firm serves consumers around the country—billions have been recovered in lawsuits with which we’ve been involved.

Call Moll Law Group About an Abbott Trifecta Valve Lawsuit

Some patients with diseased aortic heart valves or who have malfunctioning or damaged prosthetic aortic heart valves were treated with Trifecta and Trifecta Valve GT. The FDA first approved first generation Trifecta valves in 2011. While the first generation model is no longer in service, many other kinds of Trifecta Valves have been implanted since. Studies show that the Abbott Trifecta Valves require more reintervention than other commercial valves. They’ve deteriorated in some instances just three to four years after being implanted.

Health care providers have been told about the potential dangers of early structural valve deterioration (SVD), but the full risks are not known. If you were harmed by a valve or a loved one died because of the deterioration of an Abbott Trifecta Valve, you should let the FDA know about the adverse event, so that it can get a better sense of the dangers. You can also expect that your health care provider is now aware of the possible risks and if you have one implanted, you should see your provider to determine the next best steps.

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Published on: January 28, 2025

Study Reveals Increase in Pregnancy Complications in Illinois

By Moll Law Group

woman-1284353_640-e1737155490309 Recently, Northwestern Medicine published a study that finds that maternal health problems and birth complications have increased in Illinois. Severe maternal morbidity or severe health impacts from labor and delivery went up from 1.4% to 2% in connection with 988,000 births between 2016-2023 at more than at 127 hospitals in Illinois. In addition, researchers found increased rates of gestational diabetes, mental health problems, obesity, and high blood pressure, all of which are risk factors for maternal morbidity and complications around birth. Some of the increase may have to do with medical errors. If you were harmed or lost a loved one due to what you believe was a medical error, you should call the seasoned medical malpractice lawyers of Moll Law Group. Billions have been recovered in cases with which we’ve been involved.

Consult Seasoned Attorneys of Moll Law Group About Pregnancy Complications

Doctors are aware of the stress pregnancy places on the body. Sometimes chronic illnesses and conditions can be exacerbated by pregnancy and the hormonal changes involved. In the study, which was published in the journal Obstetrics & Gynecology Open, researchers found that Black women have over twice the rate of serious complications that white women do. Also facing greater risks of severe maternal complications across racial groups are those pregnant women who live in high-poverty neighborhoods. The study found an increase of over 22% in vaginal birth complications and an increase of almost 49% with cesarean birth complications.

According to the study, greater access to prenatal care and health counseling prior to pregnancy would be a crucial move towards reducing maternal health problems and birth complications. When a mother has medical conditions during pregnancy, doctors may need to make changes to the usual recommendations for what sorts of tests are performed, what medications are taken, or how delivery is timed. The study’s authors also highlighted the work of Illinois Perinatal Quality Collaborative to reduce maternal disparities during labor and delivery and noted that increased access to doulas and patient navigator programs—and policies to reduce poverty—can also have a positive impact.

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Published on: January 21, 2025

Preterm Infant Formula Litigation Update

By Moll Law Group

Two preterm formula cases have been tried against manufacturers. The president of the American Academy of Pediatrics has emphasized that preterm infant formula is both routine and necessary in the care of preterm infants. However, last year, there was a major victory in Gill v. Abbott Laboratories, a preterm infant formula case, and hundreds of cases continue. If your baby was injured or died as a result of NEC that you believe was caused by preterm infant formula, call the seasoned Chicago-based lawyers of Moll Law Group. Billions have been recovered in cases around the country with which we’ve been involved.

Call Moll Law Group About Your Preterm Infant Formula Claim

In Gill v. Abbott Laboratories, the plaintiff sued Abbott Laboratories on behalf of her preterm infant, claiming that the company’s cow’s milk-based preterm infant formula caused the infant’s necrotizing enterocolitis (“NEC”), an intestinal disease that often affects preterm infants. The science can be a little difficult to understand since the studies say that preterm infants exclusively fed the cow’s milk-based formula are at a higher risk of developing NEC than those fed only human milk, but studies have not firmly concluded that there is a direct causal link between NEC and cow’s milk-based formula.

During Gill v. Abbott Laboratories’ pre-trial motions and pleadings, the manufacturer defended itself under the learned intermediary doctrine, an affirmative defense. This is a doctrine that applies in some states to remove responsibility from manufacturers of prescription drugs and medical devices of the duty to provide direct warnings to patients or consumers of the risks associated with those drugs and medical devices, so long as the manufacturer gives appropriate information to the physician prescribing the medication or device. The physician then bears the responsibility of letting patients know what the pros and cons are, and what would be the most prudent course of treatment. In Gill, the plaintiff moved for summary judgment and asked the court to determine that the manufacturer wasn’t entitled to use the learned intermediary doctrine and other similar affirmative defenses.

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Published on: January 7, 2025

Wrongful Death Lawsuit Against Monsanto

By Moll Law Group

agriculture-8275498_640-e1734908560378 Roundup litigation continues. One of the more recent federal lawsuits in the Roundup lawsuits involves a widow suing Monsanto Co. on the grounds that Roundup, the herbicide/weed killer is “defective, dangerous to human health, unfit and unsuitable” and should not be marketed or sold. Her lawsuit alleges that use of Roundup contributed to her late husband’s death due to Non-Hodgkin’s lymphoma. If your loved one died due to Monsanto’s Roundup, you should call the seasoned lawyers of Moll Law Group.

Call Moll Law Group About Your Claim

The lawsuit alleges that Monsanto knew or should have known that glyphosate, which is the active ingredient in the weedkiller was linked with an increased risk of developing Non-Hodgkin’s lymphoma and other types of cancer. According to the complaint, the manufacturer knew of the association all the way back to the early to mi-80s, and that since then multiple studies have revealed that glyphosate is carcinogenic. Accordingly, it’s argued in the lawsuit, the harm caused by Roundup was avoidable. The International Agency for Research on Cancer classified glyphosate as probably carcinogenic as far back as 2015.

The plaintiff claims that the company downplayed the risks, too. The marketing language that she takes exception to compares Roundup to table salt in comments about its safety, and the complaint states that there is tremendous evidence to the contrary. Theories of recovery she asserts include strict products liability, negligence, and breach of implied warranties

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Published on: December 24, 2024

Consumers are Urged Not To Use Fire Pits That Use Pooled Alcohol or Liquid Fuel

By Moll Law Group

fire-pit-6639144_640-e1734907259336 Firepits that function by burning liquid fuels like pooled alcohol can be extremely dangerous. The United States Consumer Product Safety Commission (CPSC) has asked consumers not to buy or use these fire pits, which are sold as fire pots, tabletop fire pits, miniature fireplaces and portable fires that can be used indoors. The CPSC has also asked sellers to stop selling them. They released a flame jetting safety video. Since 2019, these pits have been connected to two deaths and a minimum of 60 injuries. If you were injured or a loved one was killed as a result of burns from a firepit, 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.

Consult an Experienced Chicago-Based Product Liability Attorney

The CPSC previously alerted consumers that they should not use FLIKRFIRE Tabletop Fireplaces and recalled Colsen-branded tabletop fire pits. With this latest warning, they’re focused on fire pits that necessitate the pouring of rubbing alcohol or another liquid fuel into an open container and the igniting of that pooled liquid. The warning specifies that this method violates the voluntary safety standard ASTM F3363-19. This standard is intended to stop pool fires where flames burn on the surface of a flammable liquid and flame jetting, which happens when flames arise in containers of liquid fuel. Rubbing alcohol, ethanol, bioethanol and similar liquids have temperatures that exceed 1600 degrees Fahrenheit. They can result in 3^rd degree burns in under a second.

When of a pool of alcohol is ignited in an open container of a fire pit, the fire can quickly get out of control. Large hot flames, greater than those expected, may go beyond the bounds of the fire pit. With flame jetting, a person who refills the alcohol or other liquid while the flame is present, can be at risk of serious burns, as well, from an explosion that propels the flames and burning hot liquid to those in the vicinity.

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Published on: December 17, 2024

Oxbryta Litigation Has Commenced

By Moll Law Group

treatment-4099432_6402-e1734460206805 Recently, a medication for sickle cell disease, Oxbryta, was voluntarily recalled because it can cause complications and death. Litigation has begun against Pfizer Inc. and its subsidiary Global Therapeutics. One plaintiff, a patient who underwent treatment, has alleged that the companies should have known that administration of the sickle cell treatment could result in a patient’s death. According to that plaintiff, he suffered a higher rate of vaso-occlusive crisis after he used the medication. Pfizer denies that it acted irresponsibly. If you were harmed by Oxbryta, give the seasoned Chicago-based dangerous drug lawyers of Moll Law Group a call.

Call Moll Law Group About Your Oxbryta Claim

Oxbryta is a drug that was meant to alleviate sick cell disease symptoms. It was formulated to prevent hemoglobin polymerization; this, in turn, stops the sickling of red blood cells and improving the ability for hemoglobin to be oxygenated. In 2019, the Food and Drug Administration (FDA) accelerated its approval for those patients who are at least 12-years-old. In 2021, the FDA approved the drug for children with the minimum age for use being age 4. Unfortunately, once the drug was used in the real world, certain side effects were dire. One of the complications that arose in connection with the drug were vaso-occlusive crises, painful incidents where the sickled blood cells obstruct the flow of blood through a patient’s body. Some patients died as a result of these complications.

Pfizer recalled the drug across the world in September 2024, due to this real-world data that indicated Oxbryta’s risks are greater than its potential benefits. Patients and family members brought many lawsuits against Pfizer, and many of these claimed that Pfizer and its subsidiary had failed to provide adequate warnings as to these risks and complications. In plain terms, they are arguing that the company didn’t let them know about the risk of suffering vaso-occlusive crises and death and this prevented doctors and patients from making informed decisions about whether or not to take the drug.

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Published on: December 3, 2024

Around 222,000 Bed Rails Have Been Recalled by Medical King

By Moll Law Group

bed-5985434_640-e1732641943482 Recently, manufacturer Home4U, which does business as Medical King and the United States Product Safety Commission (CPSC) recalled around 222,000 adult portable bedrails because the product carries the threat of serious entrapment and asphyxia. People using the bedrails can get trapped between the bed and the rail or may find themselves between the mattress and the rail. One man has died in connection with the affected bedrails. If you were injured or a loved one suffered entrapment or were asphyxiated as a result of one of the Medical King bedrails, call the experienced Chicago-based attorneys of Moll Law Group. Billions have been recovered in lawsuits around the country with which we’ve been involved. We represent clients nationwide.

Consult Moll Law Group About Your Bed Rail Claim

Between January 2020-March 2024, around 222,000 bed rails made by Medical King were sold for $40 at medicalkingusa.com, Amazon.com, Target Plus, Walmart.com, eBay, and Kohls.com were recalled. Made in China, the bedrails that have been recalled are the Medical King Bed Assist Rail Without Legs (model number 7037) and Medical King’s Bed Assist Rail with Adjustable Heights (model numbers 7007 and 7057). The one with no legs has a silver metal tube construction, a black fabric pouch, and a black foam rubber grip handle. The one with adjustable heights is composed of white or black metal tubing and has a black foam rubber grip handle, plus fabric pouch.

As a result of a recalled Medical King bed rail (the Bed Assist Rail with Adjustable Heights, model number 7007), a 66-year-old was entrapped by the bed rail against a mattress and died. If you or a loved one is using a recalled bed rail, it is imperative to stop using it. You can get a free repair kit or replacement bed rail by contacting the manufacturer.

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Published on: November 26, 2024

People in 18 States May Have Gotten Sick From Carrots Contaminated With E. coli

By Moll Law Group

carrot-2309814_640-e1732640911160 The Centers for Disease Control has announced a multistate outbreak of E. coli O121 infections linked to supplier Grimmway Farms bagged recalled, organic carrots and baby carrots, which were sold under several brand names. One person has died and at least 38 people have become ill after the outbreak. The actual numbers may be much higher. The Food and Drug Administration has publicly stated that the carrots may have been contaminated with the Shiga toxin-producing kind of E. coli, which most affects children age 5 years or under and adults who are 65 years or older If you suffered E.coli due to contaminated carrots, you should call the seasoned Chicago-based lawyers of Moll Law Group to learn your legal options. We represent clients around the country and have experience pursuing damages on behalf of those injured by contaminated foods or defective products.

Consult Moll Law Group About Your Food Safety Claim

On November 16, 2024, Grimmway Farms recalled multiples sizes and brands of bagged organic baby and whole carrots due to risk of E.coli contamination. The known cases of E.coli happened in 18 states and from September 6, 2024-October 28, 2024. It’s most likely, officials says, that the carrots being sold in the grocery store now are not affected, but carrots you have in your home might be, even if you’re not in one of those 18 states but are anywhere in the country. It’s important to throw those bagged, organic carrots away and not consume them or return them to the place you bought them.

These products are likely no longer in stores for sale but may still be in your home. The CDC advises throwing away any recalled organic carrots that are in your freezer or refrigerator. You should also wash and sanitize anything that touched them in the dishwasher or by using soap and hot or boiling water. Be on the lookout for serious symptoms. If you have signs of dehydration such as dizziness; diarrhea for more than 3 days that doesn’t improve; vomiting that is so significant you can’t even keep down liquids; or a fever that exceeds 102 degrees, Fahrenheit, you should call your doctor, as these are considered serious E. coli symptoms.

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Published on: November 19, 2024

Two Valisure Studies Find Cancer Risk in Acne Creams and Facewash

By Moll Law Group

hand-washing-4818792_640 Recently, a second study of dozens of acne creams and cleansers, including Clearasil and Proactiv, made with benzoyl peroxide, found that they contain high levels of the carcinogen benzene. An earlier study with the same finding had been criticized for its methodology; however the second study confirming those findings sounds an alarm that federal agencies should pay attention to. Senator Richard Blumenthal has called on the FDA to investigate the carcinogen levels in acne treatments. If you were harmed or believe that you developed cancer due to an acne cream, facewash, or cleanser you should call the seasoned Chicago-based dangerous drug attorneys of Moll Law Group. We represent clients nationwide, and billions have been recovered in lawsuits with which we’ve been involved.

Consult Moll Law Group About Your Acne Cream or Cleanser Lawsuit

A first study of the acne creams and facewashes by Valisure found that high levels of benzene could form in benzoyl peroxide products, but the study had been criticized for testing products that were maintained at the high temperature of 122 degrees Fahrenheit. In March, Valisure had petitioned the FDA to recall those acne creams and cleansers that had large quantities of benzene. The FDA had said it wanted to verify the lab’s claims, and in the summer, a spokesperson stated that the agency was still researching the issue.

In the second study, more than 100 benzoyl peroxide acne creams, face washes and other products were tested. The tested products were those that are available at major stores in six states: California, Connecticut, Florida, Illinois, New York, and Texas. Unlike with the earlier study, these products were kept at room temperature. Around one-third of these products contained large quantities of benzene, which is linked to developing cancer. For instance, researchers found that Proactiv included 18 times the amount of benzene that’s allowed in U.S. drugs. And researchers found that a face wash made by CVS had 13 times the levels of the carcinogen that the FDA believes is safe.

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Published on: November 12, 2024

E. Coli Outbreak Causes McDonald’s to Take Quarter Pounder Off Menu

By Moll Law Group

hamburger-2201748_640-e1731427742435 Due to an E.coli outbreak that’s made 50 people in 10 states ill and killed one person, McDonald’s has taken its quarter pounder hamburger off the menu at around 1/5^th of its restaurants in the country. Federal health officials are investigating the outbreak. Within the relevant time frame the fast food restaurant had sold around 1 million quarter pounders. The restaurant believes that more people would have gotten sick had the problem been the patties; it suggested that the onions included in the hamburger might be what’s contaminated. If you were made sick by a McDonald’s quarter pounder, you should call the seasoned Chicago-based product liability lawyers of Moll Law Group. We represent clients nationwide and billions of dollars have been recovered in cases with which we’ve been involved.

Consult Moll Law Group About Your Quarter Pounder Lawsuit

The United States Centers for Disease Control and Prevention has linked the McDonald’s quarter pounder hamburgers to an E. coli outbreak. According to the fast food chain’s North American chief supply officer, the company’s initial look into the problem has yielded the discovery that the onions used in the burger, rather than the meat, may be what’s contaminated with E. coli. The chain restaurant pointed out that its burgers are cooked at 175 degrees. E. coli is killed when food is cooked at 160 degrees, but the slivered onions, which came from one supplier, were not cooked.

To address the finding, McDonald’s has removed slivered onions and quarter pound beef patties from its restaurants in various Western states. The onion supplier, Taylor Farms, told the media that it tests both raw and finished products and didn’t find E. coli. Even so, they removed yellow onions from what was produced at their Colorado facility.

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