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Articles Posted in Product Liability

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Thousands of women have come forward to bring lawsuits against the makers of transvaginal mesh products, alleging that they suffered serious, painful, and in some cases permanent injuries as a result of the products’ dangerous nature. Ethicon is one of the main manufacturers implicated in these lawsuits, which is a subsidiary of major health product manufacturer Johnson & Johnson.

In general, these lawsuits claim that after receiving an Ethicon transvaginal mesh implant, the women experienced a variety of adverse effects, including abdominal pain, painful intercourse, and other complications as the result of the device migrating after implantation or otherwise not functioning as promised in the marketing materials associated with the device. Several of these women required subsequent revision surgeries and will need constant ongoing care to monitor the resulting complications.

There have been so many lawsuits filed against Johnson & Johnson regarding the Ethicon product that the lawsuits have been organized into an MDL or multi-district litigation. Similar to a class action, an MDL proceeding seeks to associate cases that have common facts, legal claims, and injuries. This helps expedite the processing of these cases and promotes consistency in how each case is adjudicated.

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California’s Office of Environmental Health Hazard Assessment has released a new set of revisions to its proposed overhaul of the state’s Prop 65 product labeling law. This effort is the first significant modification to the label, which must be appended to certain products and product shelf spaces, in several decades. The new warning label has been under development since 2013.

According to Prop 65, manufacturers must label products that contain a significant level of toxic chemicals deemed to pose health hazards to consumers, particularly cancer. Similarly, retailers must include a notice on shelving next to these products, further alerting consumers about the potential risks. As a result, manufacturers and product sellers doing business in California must conduct thorough tests and investigations into the chemicals that are present in their products.

OEHHA administers Prop 65 in California and maintains a list of the toxic chemicals that will require a manufacturer to include a warning. The list also provides the minimum levels at which a label will be required. In some cases, a trace amount of a toxic chemical present in a product will not require a label. There are a wide variety of chemicals on the list, including both naturally occurring and synthetic ingredients.

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The U.S. Food and Drug Administration is taking new steps to tighten the regulations on e-cigarette products, which have recently become popular based on claims that they pose less of a health risk to users than traditional tobacco products. According to the federal agency, e-cigarettes, as well as pipe tobacco, cigars, and hookah tobacco, will now be regulated according to the existing rules for smokeless tobacco, cigarettes, and roll-your-own smoking products. The new regulations will take effect 90 days from the date the new rule was enacted, which is August 3, 2016.

Under the new rules, tobacco companies will be required to submit information about their e-cigarette and tobacco products to the agency for pre-approval, including a list of the ingredients included in the product. They will also need to apply certain warnings on the products’ packaging and advertisements before they can begin marketing the products.

E-cigarettes consist of a handheld electronic device that vaporizes nicotine fluid held within a compartment in the device. It is also commonly referred to as vaping. E-cigarettes have been especially popular among the younger crowd.

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Johnson & Johnson, a manufacturer of controversial talc products, has stated that it intends to appeal a $55 million verdict against it awarded by a Missouri jury. The jury concluded that the product maker was liable for injuries the plaintiff sustained after using its talcum powder products, including ovarian cancer. According to the plaintiff, she used Johnson & Johnson’s talc products for several decades on her genital region. She was eventually diagnosed with ovarian cancer, requiring a hysterectomy and other related surgical procedures.

According to a statement released by Johnson & Johnson following the recent jury verdict, the manufacturer believes that the jury’s conclusion contravenes roughly 30 years of scientific studies from researchers around the world, concluding that cosmetic talc does not pose health and safety risks.

This litigation marks the second verdict against the health care company. Earlier, another jury in Missouri returned a $72 million verdict against the company in a case involving a woman who developed ovarian cancer and died after using Johnson & Johnson’s Baby Powder and Shower to Shower products for multiple decades. In 2013, a South Dakota jury returned a mixed verdict in another case involving allegations of cancer-related injuries after using the company’s talcum-based products. Although the jury concluded that Johnson & Johnson was negligent, it did not award any damages to the plaintiff because her cancer had gone into remission when the trial commenced.

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Cannabis is still a controversial topic in the United States. Although some states have deregulated marijuana and even allowed for recreational use, others have maintained criminal liability and punishments for the possession and distribution of marijuana. As the legal and regulatory landscape for cannabis continues to change, certain companies specializing in cannabis-based products are cropping up in states that allow medical or recreational consumption. Since this is such a new frontier, however, there are few safety measures in place to ensure that patients and patrons who purchase these products aren’t receiving a potentially dangerous product.

The federal government recently reaffirmed its long-standing position that federal prosecutors should not focus their resources on prosecuting cannabis-related crimes. In 2009, the Department of Justice issued a memo instructing federal prosecutors to forgo investigating criminal activity involving cannabis if the suspect’s conduct clearly conformed with the state’s medical marijuana laws. Five years later, Congress enacted an amendment that barred the Department of Justice from allocating federal funds to programs that would prevent states from passing legislation allowing medical marijuana.

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Nestle Corporation is one of the biggest food manufacturers in the world, with many people associating the brand with the chocolates and other sweets it makes. It also produces a wide variety of frozen foods under a variety of labels, including Stouffer’s, Lean Cuisine, and DiGiorno pizza. The manufacturing process for frozen foods can be quite complex and typically involves many different steps, including everything from preparing the food and packaging it to freezing it.

Recent reports indicate that Nestle has recalled roughly three million units of its frozen food products that contain spinach over fears that the spinach contains glass. A wide variety of products are affected, including pizzas, pasta dishes, lasagnas, and other popular Nestle dishes. The company has released a list of production codes that customers can use to identify whether a particular unit is part of the recall. The production code is printed on the side of the DiGiorno, Lean Cuisine, and Stouffer’s packages.

To recover compensation after suffering injuries from a dangerous product, the plaintiff must show that the product was designed in an unreasonably dangerous manner or that the particular unit the plaintiff received suffered from a defect during the manufacturing process that rendered the unit unreasonably dangerous. A food item that contains a dangerous foreign object not originally designed to be part of the food item satisfies the latter prong of this test.

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CBS news recently issued a news story stating that major car manufacturer Ford Motor Company has initiated a recall of roughly 391,000 of its Ford Ranger truck vehicles after a man riding in one of the vehicles died when one of the truck’s airbags exploded. The recall covers Ranger trucks manufactured between the years of 2004 and 2006.

According to authorities familiar with the accident, the decedent was driving his Ford Ranger pickup when he collided with a cow that had found its way onto the road. After making contact with the cow, the man lost control of the vehicle and collided into a fence. It is unclear whether the airbag deployed when the truck collided with the cow or when the truck collided with the fence. Reports prepared about the incident indicate that the man died as a result of metal shrapnel impaling his neck and that the shrapnel was created when the activator in the airbag exploded instead of inflating the device. The investigation also suggested that but for the defective airbag device the collision would have been moderate and unlikely to have resulted in the driver’s death.

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Johnson & Johnson, a global manufacturer of household products, was recently ordered to pay a $72 million judgment to the family of a woman who died from ovarian cancer. The decedent’s illness was linked to her use of Johnson & Johnson’s Shower to Shower and Baby Powder products over a number of decades.

The jury’s verdict included $10 million in compensatory damages and a whopping $62 million in punitive damages, which is a special type of damages designed to punish a defendant for reckless, wanton, or willful conduct while also serving as a deterrent to other companies and actors.

The lawsuit alleged that the company failed to provide warnings about the potential risk of developing cancer associated with its talcum powder products in order to increase product sales and profits. According to evidence offered at trial, Johnson & Johnson knew that its talcum powder products posed the risk of cancer as early as the 1980s, but it failed to disclose this information to the general public or regulatory officials.

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It seems like there is a never-ending stream of dietary health supplements hitting the market each day. While many of these supplements are considered hot trends or major miracle breakthroughs that can remedy a variety of ailments, they can also pose serious health risks to consumers. There have also been too many major news events involving dietary supplements that were so dangerous they had to be removed from the market entirely.

Recently, the U.S. Food and Drug Administration (FDA) issued eight separate warning letters to companies that manufacture products containing cannabidiol (CBD) that are intended for use as dietary supplements. According to these warning letters, the companies’ claims that the CBD-containing products can help treat certain conditions like cancer, lupus, post-traumatic stress disorder, and other ailments were not appropriately verified by the FDA.

CBD products are non-narcotics containing ingredients derived from cannabis sativa, a plant that is also used to make the narcotic drug marijuana. Although some states have decriminalized and even legalized marijuana consumption, it remains illegal on the federal level.

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There are hundreds of thousands of products in our modern, consumer-driven world. While many of these are products that we may select and purchase of our own accord, there are numerous other products that we are forced to encounter on a daily basis. Regardless of the circumstance, products can pose a serious danger to the health and safety of you and your family.

Every state has adopted a consumer protection law that allows consumers who suffer injuries due to a dangerous product to bring a claim against the manufacturer and other potentially liable parties. Although there are some differences in these laws, they generally impose the same requirements on plaintiffs seeking compensation from a product manufacturer or distributor.

In general, product makers owe the public a duty to design products that are reasonably safe and to ensure that individual products on the manufacturing line do not suffer from defects that render them unreasonably dangerous. The product liability laws also impose liability against defendants who fail to provide an adequate warning about certain dangers that a product may pose, or who fail to provide sufficient instructions for using the product in a safe and reasonable manner.

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