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100+ articles of harm and corruption by Johnson & Johnson and subsidiary products.
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Hi All,
This is INDEPENDENT work that you are certainly NOT going to see in conventional media.
Gifts of support are always very much appreciated...
 
Thank you,
Emily
 
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Lawsuits Mounting for Harm by Johnson & Johnson Implanted Mesh Products
J&J started using a mesh product for organ prolapse, such as bladder and uterous. However, the consequences of this option increases risks of harm to other internal organs.

Keywords: jnj, johnson and johnson, johnson + johnson, J&J, gynecare, prolift, mesh, vaginal
Date Created/Edited: 2012, May 3
 

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ACA the Affordable CORRUPTION Act
The only purpose of the ACA/ObamaCare was to force everyone to pay legal fees and victim settlements and care from harm by Johnson & Johnson.
 
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Mesh Files
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Why President Trump Should Shut Down US FDA (2017, March 28)
Healthcare organizations around the world depend on US FDA decisions, however, profit, rather than safety, seems to be the primary motivation.
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The Difference Between Guinea Pig and Cash Cow (2016, September 27)
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Johnson & Johnson Victims at Risk of RE-Victimization (2016, August 22)
If you are currently a victim of a known harmful Johnson & Johnson subsidiary product and have high medical needs due to your injuries, you are at increased risk of becoming a victim of another known harmful Johnson & Johnson subsidiary product.
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Johnson & Johnson Animas Defective Diabetes Devices (2016, August 4)
Gosh and golly gee willikers, yet another Johnson & Johnson subsidiary, Animas, totally sucks, jah?
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Johnson & Johnson Ethicrap, I Mean EthiCON, More JNJ JUNK (2016, July 25)
As I've mentioned, Johnson & Johnson has so many bad products I have to put a bunch in each article now to try to keep up. Now for EthiCON crap.
Johnson and Johnson, Johnson & Johnson, ethicon, harmonic ace, morcellator, physiomesh, secure strap, stapler
 
Mesh implants are made to support organs to correct incontinence and pelvic organ prolapse - a condition that affects women. They are basically a mesh sling to hold the organs in position.
 
In 1998, two years after the Boston Scientific product was approved by the FDA, according to Bloomberg, "J&J Mesh Approved by FDA Based on Recalled Device", J&J created a mesh product under the Johnson & Johnson brand. The new device easily passed through the FDA using the 510(k) loophole. In this loophole, if the new product is substantially equivalent to an existing product, the product is approved without additional and costly testing. Although I have seen many media articles stating that the mesh devices sold and implanted in people were sold for three years without FDA approval, that is not entirely accurate. The device was approved by the FDA based on the fact that the device was nearly identical to an existing product.
 

 

In 1999, due to high failure and deterioration rates in patients who received the device, Boston Scientific issued a recall and stopped distributing the mesh product. However, Johnson & Johnson, and at least one other company, continue to sell a device with known risks of harm to the patients who receive the implants.
 
Currenty, there are more than 600 lawsuits pending from people harmed by TVT Mesh manufactured by Johnson & Johnson and other companies, as reported by NewsInferno: First Bard Avaulta Transvaginal Mesh Lawsuit Scheduled for February Trial in MDL.
 
Resources:
1. Alex Nussbaum and David Voreacos (2011, October 27). J&J Mesh Approved by FDA Based on Recalled Device Bloomberg. Retrieved from http://www.bloomberg.com/news/2011-10-20/j-j-vaginal-mesh-approved-by-fda-based-on-older-recalled-device.html
 
2. Laurie Villanueva (2012, May 3). First Bard Avaulta Transvaginal Mesh Lawsuit Scheduled for February Trial in MDL News Inferno. Retrieved from http://www.newsinferno.com/first-bard-avaulta-transvaginal-mesh-lawsuit-scheduled-for-february-trial-in-mdl/
 
 
 
 
 
 
 
 
 
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