LANA C. KEETON PRESENTATION "THE INTERSECTION OF MEDICINE & LAW" 09/05/2018 TO FDA'S CDRH 87,000 UN-REPORTED TRANSVAGINAL MESH ADVERSE REPORTS MADE BY MS. KEETON

LANA C. KEETON

© 2005 - 2018 Lana C. Keeton All rights reserved. 09/05/2018

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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 3^rd 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.