People go to hospitals and medical professionals for viable solutions. They go because they want things to improve. They want things to get better. What happens when the very thing that was suppose to help, makes things worse? What are the actual clinical trails for these devices? Do they have any oversight whatsoever or are they simply allowed to be in the market with no serious oversight by the FDA? The medical device industry makes the pharmaceutical industry look like a dinosaur. What are the benefits of pushing these devices on the market without considering the risks? Most pharmaceutical professionals will tell you that if a drug has not been on the market for 7 to 10 years you are the experiment. Why are these defective devices being recalled if they went through clinical trail? Share your comments with the community by posting below. Share the wealth of health with your friends and family by sharing this article with 3 people today. As always you are the best part of what we do. Keep sharing!
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