Articles Tagged with product liability

Medical device failures occur more often than most people realize, and they can have catastrophic effects on the health of the individuals who were supposed to be helped by them. 

Lawsuits for medical device failures often fall under the category of product liability law. However, medical malpractice lawsuits often include medical device failure as part of the suit. For instance, if a device had a known or knowable defect and the medical provider used it anyway, both the provider and the manufacturer would be held at fault for your injuries.

If you believe you have been injured by a faulty medical device, don’t wait to seek the help of an experienced personal injury lawyer. As a Florida personal injury attorney, I have expertise in all aspects of medical malpractice and product liability law, and I am committed to helping Florida residents throughout the state receive just and fair compensation to help them cope with the injuries they have sustained through someone else’s negligence.

There are three types of product liability claims: defective design, defective manufacture, and failure to warn or instruct. You or a loved one can be injured by any type of product: a vehicle, household item, toy, recreational item, medical device, pharmaceutical or over-the-counter drug, or any other man-made product. As a Florida personal injury lawyer, I have helped many clients injured by a wide variety of products recover damages to compensate them for the injuries, loss of income, expenses, and pain and suffering caused by a company’s negligence.

Defective design

If a product is designed poorly, it could increase the risk of injury even during proper use of the item. Defective design is often the cause of many auto recalls, but unfortunately, some of those defects are not discovered – or at least not reported – until someone gets hurt. An electric blanket’s design may cause burns when set at the highest temperature or may short out, causing burns. Power tools may not include safety features, which exist but were not included in the design. Products designed for children may be choking hazards.

Mounjaro, manufactured by Eli Lilly and Co., is an injectable prescription medicine that is used along with diet and exercise to improve blood sugar in adults with type 2 diabetes mellitus. Mounjaro received FDA approval in May of 2022. 

Mounjaro is a glucagon-like peptide-1 (GLP-1) receptor agonist, like Ozempic, which is produced by Novo Nordisk. In addition, Mounjaro also activates glucose-dependent insulinotropic peptide (GIP), a hormone that helps release insulin after consumption.

Eli Lilly claims on the Mounjaro website that studies showed 3 out of 4 people reached an A1C under 7%, from an average starting at 7.9% to 8.6%.

Ozempic is a prescription drug designed for treating type 2 diabetes. It is also being used off-label for weight loss. Like all pharmaceuticals, Ozempic has a list of side effects, but some people are now suing Ozempic for serious injury not listed as a potential risk. If you have taken Ozempic and believe it has adversely impacted you, please call our office to discuss the details.  

About Ozempic

Ozempic is made by Novo Nordisk, a Danish company that was founded 100 years ago to make the newly-discovered drug, insulin, for patients with diabetes. Ozempic, the brand name for semaglutide, is a glucagon-like peptide-1 (GLP-1) analog that received FDA approval on December 5, 2017.

Airbags are a tremendous development in automobile safety, saving untold lives every year. But when they don’t work properly, the passengers and drivers are not protected, and the defective airbags themselves can, in fact, cause harm. It’s important to check your manufacturer’s recalls to determine if your car is safe. If you have already been injured by faulty airbags and you are a resident of Florida, I may be able to help you receive the compensation you deserve for their negligence. 

 2023 Toyota and Lexus airbag recall

The most recent recall, July 2023, is the recall of over 110,000 Toyota and Lexus vehicles to repair faulty wiring in the steering column. Apparently, an electrical connection was not welded properly at the factory. The cable within the column could detach, disabling the driver-side airbag and causing the airbag light to be illumined. 

The news is full of examples of major companies being sued for damage caused by their products. As a Florida personal injury lawyer, I help individuals fight against big corporations and their teams of lawyers in order to guarantee that those hurt by the negligence of others receive the compensation they deserve.

What is an MDL case?

A multidistrict lawsuit (MDL) refers to a mass tort, or a circumstance in which many people are suing a manufacturer over the same product. To simplify the process and keep the court system from being overwhelmed, the U.S. Judicial Panel on Multidistrict Litigation (JPML) may determine that a certain type of case should be handled as an MDL, in which a single judge is appointed to oversee the discovery, pre-trial motions, and settlement conferences since the processes would be similar in all cases. 

Essure birth control implants and 3M Earplugs are two recent high-profile product liability cases in which tens of thousands of users who were injured sued for damages. In both these cases, the sheer volume of lawsuits would swamp the courts if taken individually, thus they are class-action lawsuits. 

Essure’s manufacturer, Bayer Healthcare, received nearly 40,000 lawsuits for its permanent birth control device by 2019 when it was pulled from the market. Bayer has recently settled a portion of these lawsuits with a $1.6 billion settlement. 

3M Company has received nearly 250,000 claims against its Combat Arms earplugs, which were standard issue to our servicemen and women between 2004 and 2015 but were ineffective as ear protection. New claims are constantly being filed, which have been consolidated into a multi-district lawsuit (MDL) before a U.S. District Judge in Florida in preparation for trial next year.

Products sold to consumers are supposed to be safe. There are many safety standards that need to be met, but often, either they are not met or the standards are not sufficient. Many defective products are recalled each year, and many others are never recalled, but still cause harm. 

Some defective products can cause burn and fire hazards, such as space heaters, electric blankets, lithium batteries, vaping equipment, and sprays such as PAM. 

Defective gym and sports equipment can cause serious physical injury due to the collapse or tipping of an exercise machine, failure of a pulley or weight locks, or poor safety equipment such as helmets, pads, and masks.

Alec Baldwin’s accidental shooting of cinematographer Halyna Hutchins on the set of a Western movie he was filming highlights the dangers of mishandling a gun and the problem with defects in deadly weapons. Accidental injury and death from firearms are sadly fairly common and can be attributed to human error, product defect, or both.

 Product defect

A number of guns have histories of malfunction. For instance, the Sig Sauer P320 handgun can accidentally discharge when bumped or dropped or when an object touches it in a certain way. They have even gone off when holstered. A Philadelphia SEPTA police officer’s holstered gun went off on a crowded train, narrowly missing injuring riders. Several soldiers have had their holstered firearms go off, injuring them in their legs. The P320 is also known to fire if it is dropped and lands at a certain angle. Numerous other lawsuits of this type have been filed against Sig Sauer. 

Here in Florida, the Sunshine State, people use a lot of sunscreen. We are told that it protects us from the harmful rays of the sun, but recent research suggests that the sunscreen itself might be harming us. This summer the FDA has announced that it will be closely studying the negative effects of sunscreen. In early 2021, an independent pharmaceutical testing lab, Valisure, tested 294 batches of sunscreen and other sun products and found that 78 of the batches contained benzene. The FDA is now investigating the presence of additional carcinogens.  

What is benzene?

Benzene is a known carcinogen that causes cells to malfunction in ways that can cause immunity issues, and long-term exposure to it has been linked to leukemia. It is produced naturally in crude oil and gasoline, forest fires and volcanic eruptions, and cigarette smoke. It is also used extensively in the manufacturing of plastics and synthetics and is found in lubricants, dyes, detergents, drugs, and pesticides. Research into benzene several decades ago led the federal government in 1987 to limit benzene exposure in the workplace, adopting standards 50 times lower than previous standards. But some medical experts believe the exposure limits are still too high.

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