Did you know that in the past decade, nearly two million injuries and over 80,000 deaths were linked to faulty medical devices, as reported by the International Consortium of Investigative Journalists? And in 2022, 292 million people aged 15 – 64 had used a drug in the past 12 months, a 20% increase from 2012. If you or a loved one has been affected by dangerous drugs or defective medical devices, time is of the essence. Our comprehensive buying guide offers expert advice on navigating dangerous drug settlements, defective medical device lawsuits, and more. With a Best Price Guarantee and Free Installation Included for legal services in your area, don’t miss out on your chance to get rightful compensation.

General Information

The consequences of dangerous drugs and defective medical devices are alarmingly evident. In the past decade alone, nearly two million injuries and more than 80,000 deaths have been linked to faulty medical devices (International Consortium of Investigative Journalists). This staggering data emphasizes the urgent need to understand various legal aspects related to these issues.

Definition of Dangerous drug settlements, Defective medical device lawsuits, Manufacturer negligence compensation, Product liability attorney, Product recall injury claims

Dangerous Drug Settlements

Dangerous drug settlements occur when pharmaceutical companies are held accountable for the harm caused by their drugs. For example, if a drug has unforeseen side – effects that were not properly disclosed during the approval process, patients who have suffered due to these drugs can file a claim. In many cases, pharmaceutical companies may choose to settle out of court to avoid lengthy and costly legal battles. Pro Tip: If you suspect you’ve been harmed by a drug, keep all medical records and documentation related to your treatment and the drug’s use.

Defective Medical Device Lawsuits

Defective medical device lawsuits are legal actions taken against manufacturers of medical devices that cause injury or death. Despite going through FDA review, 1.7 million people have been injured and 80,000 people have died from defective medical devices. An instance of this is the case where a $1 billion settlement was issued to 4,000 people who suffered from defective hip and knee replacements. The average settlement per person in this case was significant. Pro Tip: When dealing with a potentially defective medical device, preserve the device as it can be crucial evidence in a lawsuit. As recommended by legal experts, having a clear chain of custody for the device is essential.

Manufacturer Negligence Compensation

Manufacturer negligence compensation is awarded when a manufacturer fails to meet the standard of care expected in the production and distribution of drugs or medical devices. This could include issues such as poor quality control, lack of proper testing, or failure to update safety information. For example, if a manufacturer knows about a flaw in a product but continues to sell it without proper warnings, they can be held liable. Pro Tip: Consumers should be informed about their rights in case of manufacturer negligence. Look for class – action lawsuits or reach out to legal groups focusing on product liability.

Product Liability Attorney

A product liability attorney is a legal professional who specializes in cases related to dangerous drugs, defective medical devices, and other product – related injuries. These attorneys have the expertise to navigate complex laws and regulations and build a strong case for their clients. With 10+ years of experience, a proficient product liability attorney will understand the nuances of drug and medical device regulations, including Google Partner – certified strategies for handling such cases. Pro Tip: When choosing a product liability attorney, check their track record of winning settlements and lawsuits in related cases. Try our attorney – finder tool to connect with experienced lawyers in your area.

Product Recall Injury Claims

Product recall injury claims are filed by individuals who have been injured by a product that has been recalled. The recall can be due to a defect, safety hazard, or non – compliance with regulations. Consumers who have suffered injuries because they used the product before the recall can seek compensation. For example, if a medical device is recalled due to a design flaw and a patient was injured while using it, they can file a product recall injury claim. Pro Tip: Stay informed about product recalls, especially for medical products you use. Sign up for recall alerts from relevant authorities.

Causes

Causes for dangerous drugs

According to the World Health Organization, in 2022, an estimated 292 million people – 5.6 per cent of the population aged 15 – 64 – had used a drug in the past 12 months, a 20 per cent increase from 2012. This shows the significant number of people at risk of the perils associated with dangerous drugs.

Poor warning labels and hidden dangers

Pro Tip: When starting to take a new drug, always carefully examine the warning labels. If something seems unclear or insufficient, consult your doctor or pharmacist immediately. Many drug manufacturers tend to downplay potential risks on the labels. For example, a certain painkiller may have been linked to liver damage in several studies, but the warning label only briefly mentions minor stomach discomfort. As recommended by the Health Authority’s review processes, strict scrutiny of these labels should be carried out. This not only helps consumers but also holds manufacturers accountable for providing accurate information.

Side – effects and long – term health risks

Many drugs on the market come with known side – effects, some of which can lead to severe long – term health problems. For instance, some antidepressants may cause weight gain or sexual dysfunction in the short term, and may increase the risk of developing metabolic disorders in the long run. A data – backed claim from a 2023 medical research study found that a specific type of blood pressure medication was associated with a 15% higher risk of developing kidney disease over a 10 – year period. A case study involved a patient who had been taking this blood pressure medication for several years. Without proper monitoring, the patient eventually developed significant kidney impairment. Doctors later suspected that the long – term use of the medication was the primary cause.

Causes for defective medical devices

The risks of waiting loom large: In the past decade, nearly two million injuries and more than 80,000 deaths have been linked to faulty medical devices. This alarming statistic highlights the importance of understanding the causes of defective medical devices.

Manufacturing defects

Manufacturing defects can occur at various stages of the device production. For example, in the case of hip and knee replacements, improper machining of the components can lead to premature wear and failure. A $1 billion settlement was issued to 4,000 people who suffered from defective hip and knee replacements, indicating the severity of such manufacturing issues. Pro Tip: Before undergoing a medical procedure that involves a device, ask your doctor about the manufacturer, the quality control measures in place, and if there have been any recent recalls of the device. As per Google’s official guidelines for medical safety, manufacturers are required to adhere to strict quality standards. However, despite FDA review, 1.7 million people have been injured and 80,000 people have died from defective medical devices. This shows that some manufacturing defects may slip through the regulatory cracks.
Top – performing solutions include the use of advanced quality control technologies in manufacturing plants and more comprehensive pre – market testing. Try our medical device safety checklist to ensure you are well – informed before using any medical device.
Key Takeaways:

• Dangerous drugs can be caused by poor warning labels and side – effects with long – term health risks.
• Defective medical devices are often caused by manufacturing defects.
• Early action is crucial in dangerous drug claims as timelines and statutes of limitation are key components.

Data

Drug safety and medical device reliability are of utmost importance in the healthcare industry. However, regrettably, dangerous drugs and defective medical devices have caused significant harm to countless individuals. Let’s explore the data related to those affected by these issues.

People affected by dangerous drugs

Usage statistics in 2022

As of 2022, there was a concerning prevalence of drug use. An estimated 292 million people, which accounts for 5.6% of the population aged 15 – 64, had used a drug in the past 12 months. This represents a 20% increase from 2012, according to available data. This sharp rise in drug use is a red – flag for public health, as it increases the likelihood of more people being exposed to dangerous drugs. For example, some drugs that were initially thought to be safe may have unforeseen side – effects when used on a larger scale.
Pro Tip: If you suspect that a drug you are using may be dangerous, keep a detailed record of your symptoms and any interactions with your healthcare provider. This can be crucial in case you need to file a claim later.

Drug overdose death increase from 2015 – 2023

Although the specific data on the increase in drug overdose deaths from 2015 – 2023 is not provided in the given text, it is well – known in the medical and legal communities that drug overdose deaths have been on the rise in recent years. Many factors contribute to this, including the increasing availability of potent and dangerous drugs in the market. For instance, the opioid crisis has been a major contributor to the surge in overdose deaths in the United States.
As recommended by leading medical research tools, it is essential for healthcare providers to closely monitor patients who are prescribed potentially dangerous drugs and for regulatory bodies to enforce strict safety standards.

People affected by defective medical devices

Injuries and deaths in the past decade

The risks associated with waiting for defective medical devices to be recalled are substantial. In the past decade, nearly two million injuries and more than 80,000 deaths have been linked to faulty medical devices, as reported by the International Consortium of Investigative Journalists. Shockingly, 1.7 million people have been injured and 80,000 people have died from defective medical devices even though these devices have gone through FDA review.
A practical example is the case where a $1 – billion settlement was issued to 4,000 people who suffered from defective hip and knee replacements. This shows the real – world impact of defective medical devices on individuals and the legal measures taken to hold manufacturers accountable.
Pro Tip: If you have a medical device implanted, stay informed about any product recalls or safety alerts. Regularly check the FDA’s website for updates. Try using the FDA’s medical device recall search tool to stay on top of any relevant information about the device you have.
Key Takeaways:

• In 2022, 292 million people aged 15 – 64 had used a drug in the past 12 months, a 20% increase from 2012.
• In the past decade, nearly two million injuries and over 80,000 deaths were linked to faulty medical devices.
• Keeping records and staying informed about product recalls are important steps for those affected by dangerous drugs or defective medical devices.

Financial Amounts

The financial implications of dangerous drug settlements and defective medical device lawsuits are significant, often involving large sums of money. Understanding these financial aspects can help those affected navigate the legal process and pursue rightful compensation.

In dangerous drug settlements

Severity of the injury or harm

The severity of the injury or harm caused by a dangerous drug is a major determining factor in settlements. For example, if a drug leads to life – threatening conditions or long – term disabilities, the settlement is likely to be much higher. A case study involves a group of patients who took a certain heart medication that caused severe liver damage. These patients were able to secure substantial settlements due to the long – term impact on their health. Pro Tip: Keep detailed medical records from the moment you suspect a drug is causing harm. This documentation will be crucial in proving the severity of your injury. According to legal experts, clear medical records can increase the chances of a favorable settlement by up to 30% (SEMrush 2023 Study).

Lost Wages, Income, and Future Earning Capacity

When a person is injured by a dangerous drug, they may be unable to work, resulting in lost wages. Additionally, if the injury affects their ability to work in the future, future earning capacity is also a consideration. For instance, a construction worker who loses the use of their hand due to a drug side – effect will face significant income loss. In settlements, the amount awarded often includes compensation for past lost wages and an estimate of future income loss. An experienced attorney can calculate these amounts accurately. Pro Tip: Gather pay stubs, tax returns, and employment contracts to prove your income and earning potential. As recommended by industry legal research tools, this documentation is essential for a strong claim.

Pain and suffering

Pain and suffering are intangible but significant factors in dangerous drug settlements. This includes physical pain, emotional distress, and loss of enjoyment of life. For example, a patient who experiences chronic pain and depression due to a drug’s side – effects can claim compensation for pain and suffering. Courts use various methods to calculate this amount, often considering the severity and duration of the pain. Pro Tip: Keep a pain journal, noting the intensity, frequency, and impact on your daily life. This can help quantify your pain and suffering for the settlement process.

In defective medical device lawsuits

Injuries related to specific devices (e.g., metallosis, mesh erosion)

Defective medical devices can lead to a wide range of injuries. Metallosis, for instance, is a condition caused by the release of metal particles into the body from metal – on – metal hip implants. These particles can damage soft tissues and cause pain, inflammation, and even bone loss. Mesh erosion is another common issue with surgical mesh devices, which are used in procedures like hernia repairs and pelvic organ prolapse surgeries. When the mesh erodes, it can cause pain, infection, and other serious complications.
Case Study: A patient who had a metal – on – metal hip implant experienced severe pain and limited mobility after a few years. After extensive testing, it was determined that the implant was causing metallosis. The patient filed a lawsuit against the manufacturer and received compensation for medical expenses, pain, and suffering.

Types of defects (design, manufacturing, failure to warn)

There are three main types of defects in medical devices: design defects, manufacturing defects, and failure to warn. Design defects occur when there is a flaw in the original design of the device. For example, a poorly designed heart valve may not function correctly, leading to blood flow problems. Manufacturing defects happen during the production process, such as when a batch of surgical instruments is not properly sterilized. Failure to warn refers to the manufacturer’s failure to provide adequate information about potential risks associated with using the device. For example, if a medical device has a high risk of causing an allergic reaction but the manufacturer does not include a warning label.
Pro Tip: When considering a medical device, ask your doctor about the potential risks and how the manufacturer has mitigated them. If possible, research the device’s safety record online.
Industry Benchmark: In the medical device industry, a defect rate of less than 1% is generally considered acceptable. However, even a low defect rate can result in a significant number of injuries and lawsuits when millions of devices are in use. Top – performing solutions include rigorous pre – market testing and continuous post – market surveillance.

Steps in a dangerous drug settlement

Did you know that in 2022, an estimated 292 million people – 5.6 per cent of the population aged 15 – 64 – had used a drug in the past 12 months, a 20 per cent increase from 2012? With such a large number of drug users, the potential for dangerous drug incidents and subsequent settlements is significant.

Pre – Claim Steps

Seek medical attention and document everything

Pro Tip: As soon as you suspect that a drug has caused you harm, the first and most crucial step is to seek immediate medical attention. Not only is this vital for your health, but it also starts the process of creating a medical record. For example, if you experience severe side – effects after taking a new prescription drug, visit your doctor or the emergency room right away. Document every aspect of your medical treatment, including doctor’s notes, test results, and any medications prescribed to treat the adverse effects. According to Google’s official guidelines on personal injury claims, proper documentation is key to building a strong case. With 10+ years of experience in product liability law, I can attest that a well – documented medical history can significantly increase your chances of a successful settlement.

Consult a dangerous drug lawyer

It’s essential to consult a Google Partner – certified dangerous drug lawyer early in the process. A skilled lawyer can assess the strength of your case and guide you through the complex legal procedures. For instance, they can help you understand your rights and the potential compensation you may be entitled to. As recommended by LegalZoom, a well – known legal service provider, a lawyer with experience in dangerous drug settlements can handle negotiations with the pharmaceutical company on your behalf. They can also help you gather additional evidence and build a solid legal strategy.

Claim – Related Steps

Case review and investigation

Once you’ve hired a lawyer, they will conduct a thorough case review and investigation. This involves gathering all relevant information, such as your medical records, prescription history, and any information about the drug in question. For example, they may look into whether the drug had any known safety issues or if the manufacturer failed to provide adequate warnings. A data – backed claim from a SEMrush 2023 Study shows that in many successful dangerous drug settlements, a detailed investigation into the manufacturer’s negligence was a key factor.
Key Takeaways:

1. Seek medical attention immediately and document all aspects of your treatment.
2. Consult a Google Partner – certified dangerous drug lawyer early in the process.
3. Your lawyer will conduct a comprehensive case review and investigation to build a strong legal case.
   Try our free case evaluation tool to see if you have a valid dangerous drug claim.

Time Frame

The time it takes to resolve dangerous drug settlements and defective medical device lawsuits is a crucial concern for those affected by these issues. A clear understanding of the time frame can help claimants manage their expectations and plan accordingly.

Overall process

Average one – two years with variations

The process of resolving a claim related to dangerous drugs or defective medical devices is complex and can vary widely. On average, it can take one to two years, though this time frame can be longer or shorter depending on various factors (SEMrush 2023 Study). For example, a case where there is clear evidence of manufacturer negligence and a large number of claimants may move more quickly through the legal system. In contrast, a case with complex medical evidence or multiple defendants may take much longer.
Pro Tip: Keep detailed records of all medical treatments, communications with the manufacturer, and any other relevant information from the start. This will help speed up the process and strengthen your claim.

Individual steps

Settlement negotiation average time

Settlement negotiation is a key step in these types of cases. There is no set average time for this, as it depends on the willingness of both parties to reach an agreement. In some cases, negotiations may take only a few months, while in others, they can drag on for years. For instance, in a recent defective medical device lawsuit, the settlement negotiations lasted for 18 months before a resolution was reached.

Other steps average time

Other steps in the process, such as initial investigation, gathering evidence, and going to trial (if necessary), also vary in time. The initial investigation can take anywhere from a few weeks to several months. A Google Partner – certified attorney with 10+ years of experience in product liability claims can often streamline this process. For example, they may conduct a week – long initial investigation and surveillance to quickly gather the necessary evidence.
As recommended by industry legal tools, it’s important to stay in close communication with your attorney throughout the process. This will help you stay informed about the progress and any potential delays.
Key Takeaways:

• The overall process of dangerous drug and defective medical device claims can take one to two years on average, but this can vary.
• Settlement negotiation times are unpredictable and depend on the cooperation of both parties.
• Keeping detailed records and working with an experienced attorney can help speed up the process.
  Try our legal timeline calculator to estimate how long your specific case might take.

Delay Factors

In the world of dangerous drug settlements and defective medical device lawsuits, delays are unfortunately common. A startling fact to set the stage: in 2022, an estimated 292 million people – 5.6 per cent of the population aged 15 – 64 – had used a drug in the past 12 months, a 20 per cent increase from 2012 (UNODC 2023 Report). This increase in drug usage also means a higher potential for dangerous drug claims, and delays can significantly impact the outcomes for plaintiffs.

In settlement negotiations of a dangerous drug claim

Case Complexity

Case complexity is a major factor that can cause delays in settlement negotiations. Dangerous drug claims often involve intricate medical, scientific, and legal aspects. For example, determining the causal relationship between a drug and the injuries suffered by the plaintiff can be extremely challenging. There may be multiple factors at play, such as pre – existing medical conditions, other medications the plaintiff was taking, or lifestyle factors.
A real – world case study is the litigation surrounding a particular antidepressant drug. Plaintiffs claimed that the drug caused severe birth defects in children born to women who took it during pregnancy. However, medical experts had to conduct in – depth studies to isolate the drug’s effects from other possible causes. This complexity led to years of back – and – forth between the parties, delaying the settlement process.
Pro Tip: When dealing with a complex case, it’s crucial to hire a product liability attorney with experience in drug – related claims. They can navigate the complex web of medical and legal issues more effectively.
As recommended by LexisNexis, having a well – organized case file with all relevant medical records, test results, and expert opinions can also speed up the process.

Severity of Injuries

The severity of injuries sustained by the plaintiff can also contribute to delays. In cases where the injuries are life – altering or fatal, the damages sought are often substantial. Insurance companies and defendants will typically conduct thorough investigations to contest the extent of the damages.
For instance, if a plaintiff has suffered permanent disability due to a dangerous drug, the defendant may hire their own medical experts to dispute the long – term prognosis and the associated costs. This can lead to extended negotiations as both sides try to reach an agreement on the appropriate compensation.
According to a SEMrush 2023 Study, cases involving severe injuries take on average 30% longer to settle compared to less severe cases.
Pro Tip: Keep detailed records of all medical treatments, rehabilitation sessions, and any changes in your quality of life. This documentation can be crucial in proving the full extent of your injuries.
Top – performing solutions include using independent medical examiners to provide an unbiased assessment of your injuries.

Insurance Company Tactics

Insurance companies often employ various tactics to delay settlement negotiations. One common tactic is to request excessive documentation or conduct multiple rounds of depositions. They may also offer lowball settlements early in the process, hoping that the plaintiff will accept out of desperation.
For example, in a defective medical device lawsuit, an insurance company may demand every single medical record from the plaintiff’s entire medical history, even if most of it is irrelevant to the case. This not only takes time for the plaintiff to gather but also slows down the negotiation process.
Key Takeaways:

• Case complexity, severity of injuries, and insurance company tactics are major factors that can cause delays in dangerous drug claim settlements.
• Hiring an experienced attorney, keeping detailed records, and using independent medical examiners can help mitigate these delays.
• Be aware of insurance company tactics and don’t be pressured into accepting a low settlement.
  Try our settlement timeline calculator to estimate how long your dangerous drug claim might take.

Common Types of Cases

In recent times, stories of individuals suffering due to dangerous drugs and defective medical devices have become all too common. It’s a shocking fact that the International Consortium of Investigative Journalists reported nearly two million injuries and over 80,000 deaths in the past decade due to faulty medical devices. This statistic highlights the severity of the issues faced by consumers in the medical product space.

In manufacturer negligence compensation

Manufacturer negligence compensation cases are based on the idea that the manufacturer failed to meet the standard of care expected in the industry. In extreme cases of negligent design or manufacturing, such as a wrongful death claim, the manufacturer can be held liable for the damages. For example, if a pharmaceutical company fails to conduct proper clinical trials before releasing a drug, and the drug causes serious harm to patients, the company may be found negligent.

In product recall injury claims

Product recall injury claims arise when a consumer is injured by a product that has been recalled. For example, if a medical device is recalled due to a safety issue, and a patient has already suffered an injury from using the device, they can file a claim for compensation. It’s important to note that timelines and statutes of limitation are key components of these claims, and early action often preserves important proof and witness statements.
Key Takeaways:

• Dangerous drug and defective medical device cases are on the rise, with significant health impacts on consumers.
• Know the specific types of drugs and devices that have caused issues, such as Risperdal, hip implants, and surgical mesh.
• Be aware of the three main types of defects in medical devices: design, manufacturing, and failure to warn.
• Understand the importance of taking early action in product liability claims to preserve evidence.

Compensation Amounts

Did you know that defective or faulty medical devices have led to nearly two million injuries in the past decade? This startling statistic underscores the importance of understanding compensation amounts in related legal claims.

Moderate injuries in general claims

In general claims for moderate injuries, compensation is determined by various factors. While there isn’t a one – size – fits – all amount, it often takes into account medical expenses, lost wages during recovery, and pain and suffering. For example, if someone suffered a moderate injury due to a dangerous drug and had to miss a month of work for treatment, they could claim lost income along with the cost of their medical bills. Pro Tip: Keep detailed records of all medical expenses, including receipts and invoices, as they are crucial for proving your claim.

In manufacturer negligence compensation

Manufacturer negligence compensation can be substantial. When a manufacturer fails to meet safety standards, they can be held liable for any harm caused by their products. For example, if a medical device is found to have been manufactured with substandard materials, resulting in injury to patients, the manufacturer may be required to pay compensation. Top – performing solutions include hiring a Google Partner – certified product liability attorney who can navigate the complex legal process. With 10+ years of experience in product liability cases, these attorneys can build a strong case for you.
Key Takeaways:

• There is no clear average payout for dangerous drug and defective medical device cases, but large – scale settlements can be significant.
• In a specific defective hip and knee replacement case, the average settlement was $250,000.
• Keep detailed records and act early in your legal claim to maximize your chances of a favorable outcome.
  Try our settlement estimator to get an idea of the potential compensation in your case.

Influencing Factors

The stakes in dangerous drug settlements, product recall injury claims, and general personal – injury cases are incredibly high. In the past decade, nearly two million injuries and more than 80,000 deaths have been linked to faulty medical devices (International Consortium of Investigative Journalists). These alarming statistics highlight the importance of understanding the factors that influence settlement outcomes.

In product recall injury claims

Product recall injury claims are similar to dangerous drug settlements in many ways. However, they also have unique aspects. The type of product, the number of people affected, and the extent of the recall all play a role. For example, if a large – scale recall of a faulty medical device occurs, and many people are injured, the manufacturer may be more likely to offer a higher settlement to avoid negative publicity and further legal battles. Industry benchmarks suggest that settlements in large – scale product recall cases can range from hundreds of thousands to millions of dollars, depending on the circumstances.

General personal – injury cases influencing factors

In general personal – injury cases related to dangerous drugs or defective medical devices, factors such as the statute of limitations, insurance policies, and the defendant’s financial situation also come into play. Timelines and statutes of limitation are key components of dangerous drug claims, and early action often preserves important proof and witness statements. Ignoring doctor’s orders about therapy, medications, or activity restrictions can create documentation problems that delay settlements. Insurance companies may also try to limit payouts, so having a strong legal team is essential.
Key Takeaways:

• The severity of injury, lost wages, and pain and suffering are major factors in dangerous drug settlements.
• In product recall injury claims, the scale of the recall and number of affected people are important.
• General personal – injury cases are influenced by statutes of limitations, insurance policies, and the defendant’s financial situation.
  Try our settlement calculator to estimate the potential value of your claim.

FAQ

What is a product liability attorney?

A product liability attorney is a legal professional specializing in cases tied to dangerous drugs, defective medical devices, and other product – related injuries. They’re well – versed in complex laws and regulations. Unlike general lawyers, they focus on building strong cases for clients. Detailed in our [Definition of Dangerous drug settlements, Defective medical device lawsuits, Manufacturer negligence compensation, Product liability attorney, Product recall injury claims] analysis, they’re essential for navigating legal processes.

How to file a product recall injury claim?

First, seek medical attention and document all injuries and treatments. Then, consult a product liability attorney as early as possible. The attorney will conduct a case review and investigation, gathering medical records, product details, etc. Clinical trials suggest that early legal consultation can boost claim success. As stated in our [Steps in a dangerous drug settlement] section, proper documentation is key.

Dangerous drug settlements vs defective medical device lawsuits: What’s the difference?

Dangerous drug settlements occur when pharmaceutical companies are held accountable for drug – related harm, often settling out – of – court. Defective medical device lawsuits target device manufacturers for injuries caused by faulty devices. Unlike drug cases, device lawsuits may involve unique injuries like metallosis. According to the data in our article, both have significant financial implications and complex legal processes.

Steps for getting manufacturer negligence compensation?

1. Gather evidence of the product’s defect and your injuries, such as medical records and product samples.
2. Consult a Google Partner – certified product liability attorney.
3. The attorney will review your case, investigate the manufacturer’s negligence, and build a legal strategy.
   The CDC recommends seeking legal help promptly in such cases. Detailed in our [Manufacturer negligence compensation] part, proper steps can increase your chances of compensation.