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Birmingham, FDA, Food & Drug Administration, Health, Hip Replacement, hip resurfacing, Medicine, Nephew, NephewSmith, Smith, Smith & Nephew BHR, UNited States
Howard has put together a video outlining his problems with the damage to his health and life caused by the metallosis resulting from a Smith & Nephew BHR metal on metal hip replacement – over 10 months in hospital and over 30 operations, he is lucky to be alive.
ExcellenT CHRISTMAS PRESENT – GEE THANKS MR SMITH AND YOUR NEPHEW!!!
More from Howard:
Howard Sadwin
06:36 - Limited
Here are the written rules regarding conflict of interest: how could the Birmingham Hip Resurfacing Device have ever been pma (pre-market approval) with McMinn and company receiving 66 million pounds for a company he was a principal. This companies best reported gross earnings was 23 million pounds ???? Then once the bhr received pma approval in the USA He and Company received an additional 33 million pounds. Originally He worked for Smith and Nephew, then along the processing of the application on the bhr he suddenly became a consultant????
CFR – Code of Federal Regulations Title 21 »
(a) The Food and Drug Administration (FDA) evaluates clinical studies submitted in marketing applications, required by law, for new human drugs and biological products and marketing applications and r…
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Merry Christmas, Happy Holidays and great New Years to all, have fun and be safe.
The Birmingham was approved through the FDA PMA ( pre-marketing approval ) process, which gives it pre-emption laws as it’s protection against prosecution.
This will be a tough legal battle, if you have been hurt by this device, be tough, do not throw in the towel, fight for what has been taken away from or this type of nightmare
will continue to hurt people. It is up to me and you to see the laws are changed, the CORRUPTION is removed and Smith and Nephew are held accountable for what they have done.
Remember this company is a repeat offender of the kickback laws and they have
paid several Governments fines, including the USA, they are in court being sued by the United States of America on a whistleblower case.
They continue to market the bhr as if nothing has happened, the I ask why are their sales down in the USA and other countries dramatically???
They have recalled the liner on their R3 ace tabular hip, recalled another component on their bhmr.
Their marketing statements compare their bhr as being much more successful than
competition, yet what is there competition??? Although they out sell all other resurfacing devices, if you read the number of registered adverse complaints, you will see that the adverse numbers have increased dramatically from years passed.
Why, because as time passes from the pma approval of this device more and more innocent folks are now becoming victims of a device that can be most hazardous to one’s health.
Know that there is something inside of you that is greater than any obstacle, remember David and Goliath, this manufacture must be held accountable for the
damage, harm, pain and suffering they have caused on innocent folks, JUSTICE
needs to be served.
We are making video live voice and few other changes, will send when completed. I am away for a week or so. Spending Holidays with friends in Alabama, 1st time away in almost 5 years, needed to chill out, back after 1st stay we’ll.
Howard Sadwin 941-928-2920
Sent from my iPhone