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Earlier this month, a Missouri jury returned a verdict assessing $110 million in damages against household product maker Johnson & Johnson in a lawsuit regarding its talcum powder products. This litigation marked the fifth trial that the company has faced regarding whether or not these products lead to the development of ovarian cancer. The plaintiff in this lawsuit, a woman from Virginia, alleged that she used the company’s talc-based products for over four decades and developed ovarian cancer as a result. The plaintiff was required to undergo chemotherapy after she was diagnosed with cancer, which later spread to her liver. In her complaint, the plaintiff specifically identified Johnson & Johnson’s Shower Powder and Baby Powder products.

The talcum powder that Johnson & Johnson uses for its talc-based products is sourced from a company called Imerys Talc America. This company is owned by another company based in Paris.

Currently, there are over 2,000 lawsuits containing similar allegations pending against Johnson & Johnson. One of the primary causes of action asserted in the complaints is that Johnson & Johnson failed to provide adequate warnings regarding the potential risk of developing certain cancers from the use of its talc-based products, despite evidence available at the time the product was marketed suggesting a linkage. These lawsuits are mostly still pending in St. Louis, Missouri.

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Advancements in technology have made vast improvements in travel and transportation. Some of the biggest technological changes to how we get around are smartphones and other digital computer platforms. Nowadays, it is not uncommon for vehicles to be equipped with their own computer systems in the dashboard, which offer motorists a variety of assistance and luxury features. Now, developers are finding ways to put these technological advancements to use for driver safety.

A recent study from the National Highway Traffic Safety Agency (NHTSA) has identified some important questions regarding how smartphones and vehicles could interface in the future. The report could spur some smartphone makers to include vehicle safety technologies in their infotainment system applications. This feature would then lock out or prevent the driver from accessing certain features while he or she is operating the vehicle.

The NHTSA released another study in 2016 that discussed a safety proposal for smartphone manufacturers. It suggests that the smartphone operating systems be equipped with a Driver Mode that will prevent the driver from accessing certain features on the phone while in transit. Some of the features that would be off-limits during travel would be social media, video, web surfing, and manual text entry. The proposal also considered taking Driver Mode one step further and having it automatically activate if the driver has not engaged it prior to operating the vehicle or if the driver has not paired it with his or her vehicle.

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A Pennsylvania jury recently returned a $20 million verdict against major household product and medical device maker Johnson & Johnson in a lawsuit regarding its pelvic mesh products. The lawsuit is part of the ongoing pelvic mesh multi-district litigation (MDL), and it constituted the third bellwether trial to proceed. According to some reports, there are over 54,000 additional lawsuits pending against the company, which is the largest health care product manufacturer in the world.

MDLs are similar to class actions in that they involve grouping claims that assert similar factual allegations and legal claims. They are different from class actions, however, in that each plaintiff must still prove his or her damages. In a class action, the entire class is awarded a collective settlement that is then distributed according to amounts and procedures approved by the court. To gauge the legal soundness of the plaintiffs’ claims, bellwether trials are conducted to gauge the likely level of liability and to assess the likely damages award against the defendant. These trials are crucial indicators of how the remaining cases pending in the MDL may play out.

In the most recent case, the plaintiff alleged that she received a TVT-Secur mesh product during a surgical procedure to address her stress urinary incontinence and that the product began to erode after two months. The plaintiff stated in her complaint that she underwent three surgeries to remove the mesh product and that Johnson & Johnson marketed the product despite its risks and without providing warnings about these risks.

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Many car accidents are caused by a driver’s negligence. Often, these accidents involve the negligent driver not paying attention to the road and rear-ending the vehicle in front of them. According to recent statistics from the National Highway Traffic Safety Administration (NHTSA), rear-end collisions account for the majority of all motor vehicle accidents, comprising about 33 percent of all crashes.

Rear-end collisions are simply defined as collisions in which one vehicle collides with the rear of another vehicle. Across the country, over 2,000 rear-end collisions resulted in a fatality, and over 500,000 resulted in an injury. In Illinois, if another driver is to blame, an accident victim may recover damages from any defendant who was more at fault than they were in causing the accident.

Bachelor Star Charged with Causing Fatal Accident and Fleeing the Scene

According to one news source, a former star of the T.V. series “The Bachelor” has been charged with causing a traffic accident that killed a driver and fleeing the scene. Allegedly, the reality show star was driving a pickup truck at around 8 p.m. on a Monday evening in Iowa and rear-ended a tractor. The tractor then rolled over and fell in a ditch. The reality star’s truck fell in a ditch on the opposite side of the road. The tractor driver, a farmer, was taken to the hospital, where he was pronounced dead. He was 66 years old and is survived by his wife, two sons, and three grandchildren.

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Breast implants are one of the most popular elective surgeries throughout the world. Although breast implants have been around for several decades, the U.S. Food and Drug Administration has recently identified a possible linkage between these medical devices and anaplastic large cell lymphoma (ALCL). This condition is categorized as an uncommon type of non-Hodgkin’s lymphoma. The FDA first identified the potential connection in 2011.

Now, in 2017, the FDA has indicated that it has collected additional evidence regarding this linkage. When it first started its investigation six years ago, the FDA was only able to identify a few cases involving the development of the disease in relationship to breast implants. This made it more difficult to identify the factors that would contribute to the disease’s onset. The agency prepared a report detailing its understanding of the potential linkage and calling for the assessment of additional information and identification of additional cases.

In partnership with the World Health Organization, the FDA has now obtained additional information and data regarding the potential link between ALCL and breast implants. The World Health Organization is an international agency dedicated to improving human health throughout the world, particularly when it comes to combating diseases. The FDA’s latest announcement describes ALCL as a rare T-cell lymphoma that may develop after an individual receives breast implants.

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Medical products and devices are often used in surgical procedures and other medical treatments. In some cases, these devices can save lives. However, sometimes these devices can be dangerous and may result in more serious injuries than the injuries they are used to treat.

Pelvic mesh, sometimes called vaginal mesh or surgical mesh, is a medical device that is used in procedures to support repairing weakened or damaged tissue. The Food and Drug Administration (FDA) has warned of complications associated with surgical mesh when placed in the vagina.

In some cases, the mesh can erode and cause patients pain, infection, bleeding, and other issues. Pelvic mesh implants became common a decade ago to treat urinary incontinence, or involuntary leakage of urine. Many women experience a condition in which the bladder and other organs, weakened by childbirth, sag over time, causing incontinence. In recent years, thousands of lawsuits have been filed against Johnson & Johnson, the manufacturer of pelvic mesh, by women alleging they were harmed by the implants.

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There are several different types of claims that can be filed against nursing homes for injuries caused to residents. These claims include those based on intentional abuse, medical malpractice, and general negligence. A negligence claim is a common claim against a nursing home, and it arises from a provision of care that does not meet the standard expected of nursing homes.

Nursing homes may be liable for acts or omissions that cause injuries to residents. Nursing homes are required to exercise reasonable care in caring for and protecting residents. Thus, in general, a nursing home has to exercise the degree of care and skill normally used by other long-term care facilities under the same or similar circumstances.

Woman’s Family Claims Nursing Home Failed to Resuscitate Her After She Was Found Not Breathing

According to a news article, a family recently brought a lawsuit against a Highland Park nursing home, alleging that staff caused a woman’s death by failing to administer CPR when she was found not breathing in her bed. The resident, who was 52 years old, had diabetes and suffered from kidney failure, but she was only supposed to be at the home for a few weeks while recovering from pneumonia. Last month, a nurse went into her room at around 4 a.m. and found the woman “lifeless and not breathing.” The family alleges that the nurse misread the woman’s chart, which stated whether she wanted to be resuscitated. The family said she wanted to be resuscitated, but no one administered CPR.

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In some circumstances, going to trial is the best way for plaintiffs to obtain the compensation they deserve. But in other cases, plaintiffs may want to avoid trial and can obtain the results they want without having to wait until the end of a trial. In Illinois, a plaintiff can dismiss a claim against a defendant and resolve the case through an agreed-upon settlement. In some cases with multiple defendants, a plaintiff may be able to obtain a settlement against one defendant and proceed to trial against the others. Some settlements require court approval, while others require only the agreement of the parties involved.

If a plaintiff agrees to a settlement, the circuit court retains jurisdiction for at least 30 days over any motion seeking relief from the judgment. For example, a party can return during that time to enforce a settlement or to try to void the settlement, due to fraud or duress. After this time, the court has more limited jurisdiction over the case, but it may be able to decide certain issues related to the judgment.

Woman Injured by Discus at School Track Meet Obtains $350,000 Settlement

An 83-year-old woman and her husband were attending a high school track meet when the woman was hit by a student’s discus. According to one news source, the woman filed a lawsuit against the school and against the athletic association, alleging they failed to keep spectators safe.

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The U.S. Food and Drug Administration recently published a warning letter that it sent to St. Jude Medical, stating that the company likely downplayed the risks associated with its defibrillator batteries last fall. A defibrillator is a device that provides an electric shock to the heart in the event it begins to beat irregularly or cease beating entirely. The device is implanted in the patient’s chest and is battery powered.

The letter also indicates that St. Jude may have failed to notify management officials within the company, in addition to its medical advisory board, that these battery-related issues resulted in the death of a patient.

The letter also indicates that the agency has determined that St. Jude Medical has not taken sufficient or adequate measures to resolve the issue with the batteries. The company has 15 days to provide the FDA with a revised reporting plan.

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Major retailer Target has announced a recall of over half a million toy eggs designed to absorb water after concerns that the toys could create a blockage in a child’s stomach if they are ingested. The toys were designed and packaged for Easter.

Since the toys are designed to absorb water, if a child accidentally ingests a toy, it will swell inside the body and create an intestinal obstruction. The reports also suggested that the toy may not show up on an x-ray, making a life-threatening condition even harder to identify and treat. This could lead to serious health consequences, including severe pain, discomfort, dehydration, nausea, vomiting, and even death.

Although there appear to be no reports of injuries associated with the toy at this time, the Consumer Product Safety Commission initiated a Fast Track Recall covering some 560,000 toys. They also alerted members of the medical community and instructed parents to take adequate precautions, including not giving the toy to children and returning the product immediately.

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