JOHNSON & JOHNSON RULES THE WORLD! BILLIONS IN PROFIT CONDEMN MILLIONS TO DEATH OR PHYSICAL DESTRUCTION

On dramatically wonderful television advertisements for pharmaceuticals, in the supermarket in the baby products aisle, at the drug store in the feminine products aisle, at the hospital in the medical device inventory, in your doctors office pharmaceutical samples drawer....wherever you go, whatever you consume, whatever you think....JOHNSON & JOHNSON HAS A DEADLY PRODUCT WAITING FOR YOUR CONSUMPTION!

Johnson & Johnson is a multibillion dollar worldwide corporation headed by a group of thugs who have no compunction whatsoever when they daily destroy millions of lives, men, women and children. Johnson & Johnson is a cancerous entity, a blight on humanity.

#DeadWomenMatter @JNJ @JNJNews @JNJCares @AlexGorsky @Ethicon @Mentor @JNJInnovations #CleanUpYourMesh #JNJCriminalCorporation

Question Number 1: how many will profit from the cancerous products distributed worldwide by J&J?

1) THE FDA
2) MEMBERS OF THE POLITICAL ELITE
3) OTHER MAJOR CORPORATIONS INVESTING IN J&J, SUCH AS STATE FARM AUTOMOBILE INSURANCE COMPANY
3) DOCTORS
4) HOSPITALS
5) DRUGSTORES
6) THE COURT SYSTEMS
7) ATTORNEYS: PLAINTIFF & DEFENSE

Question Number 2: Who loses from the deadly drugs and devices manufactured and distributed worldwide by Johnson & Johnson?

Yes, you guessed it!!

1) ONLY YOU THE CONSUMER!!!

TODAY ALONE THESE ARE HEADLINES FROM THE LEGAL WORLD FROM LAW 360...HUNDREDS OF THOUSANDS ARE INJURED & NO ONE, ABSOLUTELY NO ONE, HOLDS JOHNSON & JOHNSON ACCOUNTABLE.

JOHNSON & JOHNSON RULES THE WORLD!

“Vaginal Mesh MDL Judge Sick And Tired Of Bogus Suits By Steven Trader Law360, New York “ (September 7, 2016, 7:59 PM ET) -- The Georgia federal judge overseeing multidistrict litigation that alleges a Johnson & Johnson unit's defective pelvic mesh implants caused painful infections warned plaintiffs counsel Wednesday that frivolous lawsuits will no longer be tolerated and could trigger sanctions.

U.S. District Chief Judge Clay D. Land said he has spent a considerable amount of time and judicial resources deciding summary judgments in consumer lawsuits against Mentor Corp. that plaintiffs counsel should have dismissed earlier or that should have never been brought in the first place. “Enough is enough,”...
“J&J Talc Suits Show Evidence Standards Vary Among Courts By Emily Field Law360, New York” (September 7, 2016, 5:49 PM ET) -- A New Jersey state judge's decision to toss two suits alleging that Johnson & Johnson's talcum-based products caused ovarian cancer on the heels of two major trial losses for the company in similar cases highlights the different views courts have taken on the validity of scientific evidence linking talc to the disease.

Months after Missouri state juries slammed J&J with $55 million and $72 million verdicts in suits claiming that the company's talc products caused two women to develop ovarian cancer, a New Jersey state judge found...
“J&J Hit With More Talcum Powder Ovarian Cancer Claims By Shayna Posses Law360, New York” (September 7, 2016, 7:54 PM ET) -- A Louisiana woman became the latest to allege that Johnson & Johnson’s talcum powder products caused her to develop ovarian cancer in a proposed class action filed in federal court Wednesday, days after a New Jersey state judge tossed two actions making similar claims.

Shintelle Joseph joined the slew of consumers suing over J&J's talcum powder products, contending in her Louisiana federal court suit that the company touted the products as a safe and gentle way to reduce odor and moisture all over the body without warning...

SEPTEMBER 8, 2011....3 YEARS AND COUNTING and TRANSVAGINAL MESH IS STILL ON THE MARKET!

September 8, 2011...Day One!

FDA ObGyn Advisory Panel Meeting on Synthetic Surgical Mesh implanted in the pelvis of women. Transvaginal mesh it is now called...no matter where placed, no matter the brand. All lumped into one...

Guess that's okay in a sense because ALL of them cause immeasurable harm.

When will the FDA take action to stop the harm to millions of mesh injured patients, MEN AND WOMEN ALIKE?

The medical device companies have a seemingly unending amount of time to continue the harm while Patients NEVER get a second chance. Once the mesh is in, it is permanent.

So while the mesh makers get a do over, Patients become permanently disabled pelvic cripples.

An FDA warning October 2008.

Another more serious FDA warning July 13, 2011.

The FDA mandates 522 studies to 33 companies for 99 mesh products January 2012.

The FDA puts forth the possiblity of upclassifying mesh kits manufactured for pelvic organ prolapse May 2014. Comments are accepted through July 2014.

September 8, 2014...patients are still harmed every single day while mesh companies still getting a do over.

What really needs a do over is the FDA's 510(k) Premarket Notification clearance process which allowed these products ever to be sold in the first place.

Write your Congressman. Write the FDA. Write your State authorities.

LET'S GET SYNTHETIC SURGICAL MESH OFF THE MARKET...PERMANENTLY!

NO MORE DO OVERS!