Getting old is never fun. There are parts of your body that just decide to stop working properly. Even if you are not that old you might need to have a medical device installed to help you walk, help your heart beat or help you maintain a proper sugar level. Whatever the reason, these devices can fail. They might also be the subject of a recall notice. Here are some tips for handling a medical device recall notice in Nashville.
Would it shock you to know that 8 percent of medical devices -- including things like plates, surgical mesh and screws that are meant to be inserted inside the bodies of patients -- are fakes?
You never want to hear the bad news that you need to undergo knee replacement surgery. Even if you realize this can change your life for the better, it's a major procedure that is sure to bring forth a variety of challenges.
If you opt for any type of hip replacement surgery, you expect to feel better after the procedure. Sure, there is a recovery period, but as the days go by, you hope to regain the level of health you've been expecting.
A medical device recall can typically be started by the company that made the device, as a voluntary recall, or by the government. Many companies, when they learn of issues that would mandate a recall, will simply issue it on their own to avoid having one issued by the government, but this is not always the case.
As was the case with DePuy hip replacements, the U.S. Food and Drug Administration (FDA) may order that a medical device manufacturer either temporarily or permanently remove its product from the market.
A medical device recall is every bit as serious as it sounds. When a company finds that there is a problem with one of their devices, they are expected to take immediate action. This can mean one of two things:
A heart device is every bit as important as it sounds. Any patient with one of these relies on it to improve his or her heart health, which is imperative to living a better life.
When a manufacturer becomes aware of problems with one of its medical devices, it notifies the Food and Drug Administration (FDA) that one of two actions need to happen. The first is a correction, which deals with fixing a problem where the medical device is sold or used. The second is a removal, which involves removing the medical device from where it is sold or used.
After the birth of your child, you want nothing more than for him or her to be 100 percent healthy. While this may be what you have on your mind, you never know what could actually go wrong.