Do you trust the Food and Drug Administration (FDA) to keep you informed about the dangers that crop up with medical devices, products and drugs?
When you visit your doctor's office or you end up in the emergency room, do you want the doctor looking at you or a computer screen?
When a new drug is being prepared for distribution, the Food and Drug Administration (FDA) puts it through a rigorous testing process. It's so rigorous, in fact, that patients and doctors alike complain about how long it can take for a drug that's widely available overseas to hit the market in the United States.
Patients with life-threatening allergies to peanuts, latex and other common substances often carry EpiPens for safety. EpiPens are supposed to deliver critical doses of epinephrine in an emergency so that a patient in the middle of an allergy attack could keep breathing.
Numerous defective medical devices have been the subject of alerts, warnings and recalls in other countries -- probably far more than most people realize.
Pain pumps are usually on recommended for patients who are suffering from intractable pain that hasn't responded to other forms of control.
Surgical suites are designed to be clean rooms that minimize the risk of infections developing in a patient's surgery site. Builders create these rooms with a great deal of modern technology. Ventilation systems are an important part of this technology because they direct the flow of air and any bacteria it contains away from the patient's open surgical site.
The task feels enormous and overwhelming: Making large and successful medical device manufacturers pay for harm to patients. These companies have access to a well-padded budget and to big name attorneys. How could ordinary Tennessee residents beat these odds and emerge from a lawsuit successfully?
The research and development teams involved in the creation of medical devices put a great amount of work into each project. In turn, it is safe to assume that the manufacturers of these products attempt to ensure they are safe for patient use. Unfortunately, defective medical devices can pass the development and testing phase and still cause injury to residents of Tennessee.
Despite strict safety standards and exhaustive testing procedures, defective medical devices still injure consumers. While many people may wonder how faulty devices make it past screening procedures, those injured by defective medical devices are more interested in how to remedy their situations.