LANA C. KEETON
© 2005 - 2018 Lana C. Keeton All rights reserved. 09/05/2018
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Truth in Medicine & Med Device Expert LLC
Device Expert . Legal Consultant . Patient Advocate
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“THE INTERSECTION OF MEDICINE AND LAW” Hundreds of thousands of lawsuits wind up in Multidistrict Litigation where Adverse Event Reports go to Die.
THE UNITED STATES FOOD & DRUG ADMINISTRATION CENTER FOR DEVICES & RADIOLOGIC HEALTH ADVERSE EVENT REPORTS as of SEPTEMBER 5, 2018
UNITED STATES DISTRICT COURT, S.D. WEST VIRGINIA
JOHNSON & JOHNSON/ETHICON INC 40,290 PLAINTIFFS
BOSTON SCIENTIFIC 25,282 PLAINTIFFS
AMERICAN MEDICAL SYSTEMS 21,251 PLAINTIFFS
BARD 15,694 PLAINTIFFS
COOK MEDICAL BIOLOGIC 640 PLAINTIFFS
Judge Joseph R. Goodwin issues Pretrial Order 273 in MDL02327, S.D.W.VA. Re: Johnson & Johnson/Ethicon Inc. 13,000 Transvaginal Mesh Injured Plaintiffs are dismissed without prejudice April 11, 2018 because of No Mesh Removal Surgery to remove a Permanent Implant
Today I submit a 3rd party report of over 87,000 unreported adverse events of severe injuries requiring surgical removal of the Synthetic Surgical Mesh manufactured by these 5 companies, for both Stress Urinary Incontinence and Pelvic Organ Prolapse.
THE ANSWER to these THOUSANDS OF ADVERSE EVENTS: The FDA must REMOVE TRANSVAGINAL SYNTHETIC SURGICAL MESH FROM THE MARKET IMMEDIATELY.