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THE LAW GIANT product liability lawyers:
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Medical technology has completely changed the way we experience everyday life. They have yielded longer lifespans, increased quality of life, and fewer side effects associated with medical issues. While these devices have done a lot to improve our lives, they have also caused immeasurable damage to those who are the victims of unproven or defective medical devices.
Trust The Law Giant with your legal needs while handling a device failure’s physical and mental aftermath. Schedule a consultation with The Law Giant, Personal Injury & Accident Lawyers, by calling us at (866) 523-4167 today.
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Giant Wins for All Injuries
Our personal injury lawyers handle a wide range of accidents and serious injuries across Texas.
A surprising amount of people significantly overestimate the inherent morals and ethics of medical device companies. While companies often get into this field to improve people’s lives and help people, the underlying drive is usually money. This means that when a device fails and causes severe damage to a victim, paying out the full amount the victim is owed is not their top priority.
Not only does a fair and full settlement drain their profits, but it also opens them up to further problems down the line. After all, if a faulty device damages you, it is unlikely that you are the only one impacted. When legal claims arise, medical device manufacturers do everything they can to avoid paying out the amount the victim truly deserves.
The only way to fight back against this treatment is to hire a defective medical device lawyer who knows exactly how these companies evade liability. A strong, defective medical device attorney can help you understand your rights and fight for the compensation you deserve. In some cases, an investigation uncovers evidence that a company knew about the errors in their device before they sent it to market.
You deserve the best legal representation available when you’ve been harmed by something that is supposed to help you. Let our product liability attorneys help.
AT THE LAW GIANT,
We Win Big!
With thousands of satisfied clients, our attorneys have what it takes.
Following a devastating 18-wheeler accident, our client sustained life-altering spinal injuries. By illustrating the full extent of the truck driver’s negligence and the impact on our client’s health and future, we secured essential financial relief.
Any medical component can fail and cause health issues for users. However, some of the common problems arise with the following:
The types of injuries suffered by victims vary widely, depending on the type of device they used and how long they used it without knowing it was defective. Some of the health issues we have seen among victims include:
When people place trust in their medical devices, they often believe that their medical condition is no longer an issue, as they should be able to do. However, this may lead victims to ignore symptoms and warning signs that their condition has worsened or returned. Because of this, victims may suffer irreversible damage or death due to a faulty medical component.
If you’re like most people, you may think that medical device lawsuit cases are few and far between. After all, we’ve seen the rigorous testing that vaccines and treatment options go through before being released to the public.
However, one loophole allows medical device manufacturers to bypass the thorough screening required of new devices.
The 510(k) clearance process is essentially a fast track to approval for new devices. To use this, a manufacturer must show that the new item is similar to one that already exists and is approved for use. The current product is referred to as a predicate device. Since it’s based on an existing item, the new item does not have to undergo the same testing and approval procedures as other items.
By claiming that a new product is substantially equivalent to an already-approved product, manufacturers can get their items on the market faster and make money more quickly.
This process was created to give Americans faster access to lifesaving medical devices. However, it has been primarily misused by manufacturers, who see it as a way to bypass the FDA’s scrutiny and start making money as soon as possible. Many FDA medical device recalls are for products approved via the 510(k) process.