Understanding the Complications Caused by Dangerous Medical Devices and Defective Pharmaceuticals

Thanks to the exponential advancements in technology, the pharmaceutical industry has been able to evolve in unimaginable ways for the last few decades. Today, medical professionals have access to a huge number of different devices, tools, and medications that makes addressing various health concerns a much easier task. Reliable and accessible medical solutions would be impossible without the pharmaceutical companies that continue to push the borders of innovation.

While the pharmaceutical industry has certainly created many new technologies that allow doctors to do more and more for their patients, its individual players can’t be considered completely infallible. There are plenty of defective medical devices and pharmaceuticals that are that are still widely-used in hospitals and other medical settings across the United States. As a matter of fact, the lawyers of Williams Kherkher have pointed out that a huge percentage of all product liability suits filed in America are for damages caused by medical drugs and devices.

Usually, the Food and Drug Administration is able to catch the issues that could lead to a certain medical product becoming harmful before approving it for public use. There are times, however, when the FDA’s investigations miss certain details and things fall through the cracks. When a medical product ends up being causing harm to patient’s well-being, pharmaceutical companies are expected to take immediate action by calling for a recall and working to improve the errors in their product. Unfortunately, in plenty of occasions, pharmaceutical companies don’t take action until it’s too late.

Metal-on-metal joint implants are an example of defective pharmaceuticals that have caused great harm and injury to a significant number of patients. Complications with these implants are known to cause bone and tissue damage, as well as metal toxicity in the body.


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