WORLDWIDE REGISTRY COMPLICATIONS
SYNTHETIC SURGICAL MESH
Y O U R R E G I S T R A T I O N W I L L P R E V E N T
H A R M T O O T H E R P E O P L E !
THANK YOU FOR YOUR PARTICIPATION!
PLEASE READ ON TO UNDERSTAND WHY THIS IS SO VERY IMPORTANT!!
The U.S. Food and Drug Administration issued a Public Health
Notification October of 2008 regarding "rare"
but serious complications of
Transvaginal Placement of Synthetic Surgical Mesh.
These complications are NOT RARE.
These complications are NOT JUST for Transvaginal Placement.
Thousands upon thousands of HERNIA REPAIRS
implanting Synthetic Surgical Mesh cause
EQUALLY as serious and as devastating complications.
Jim Shull, Lana Keeton and Bruce Rosenberg
continually pursue the FDA and the CDRH to remove
all Synthetic Surgical Meshes from the Marketplace.
Our Conference Call with Senior Members of the FDA and CDRH
(and countless e-mails, phone calls and letters from
countless sufferers of synthetic surgical mesh)
on June 16, 2008 resulted in the
Public Health Notification being issued.
Please help us continue the fight to have a
Public Health Notification issued regarding ALL
Hernia Mesh Repairs done with Synthetic Surgical Mesh!
R E G I S T E R Y O U R C O M P L I C A T I O N S BELOW....THEN PRESS SEND TO STOP OTHERS FROM BEING HARMED!
|
|