It is assumed that FDA approval indicates that all necessary testing has been done by the company before the product is released for sale to public. Why not - medical devices have to pass a rigorous pre-market approval process? So most people assume that once za devices passes through the FDA approval process, that the medical device can be safely used. But this is not always true! In fact, sometimes medical devices can be fatal.
The public has been drawn into a false sense of security in that if a medical device has been approved by the United States Food and Drug Administration, then it is safe. It has been shown time and again that FDA approved products and devices can be defective or not labeled or formulated correctly, and can cause injury. Sometimes, certain medical devices can react adversely with existing medical conditions producing dangerous side effects. Certain medical devices pose health risks to certain persons, as in the case of Gadolinium based contrast dye with person who have comprised kidney function.
If you need to file a defective product lawsuit, Anapol Schwartz is a West VA law firm on your side. Anapol Schwartz has a Wheeling attorney (Barry Hill) who can compassionately handle your defective products lawsuit.
The Manufacturers of medical devices have an obligation to test the product for such dangers. They must warn users of any potential danger associated with the use of the product. The defect may not be so obvious, and thus it is so important that the manufacturer warn.
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