J&J is being sued by approximately 65k patients in the U.S for their mesh implants despite their official statement that any mesh device as causing harm to patients as being untrue.Grab your team and tear it up in Bleeding Edge, an electrifying online brawler where every fighter comes mechanically enhanced for mayhem!Ĭhoose your fighter from a diverse cast of colourful characters from the edges of society: burn rubber as bold and beautiful Buttercup with her detachable saw blade arms, wreak havoc as Black-Metal rocker Niđhöggr with his electrifying guitar solos or slash up the streets as Daemon, New York’s most wanted assassin.Ĭome. It took this documentary for Bayer to remove Essure from the US market.ĥ. Do your own research - new isn’t better necessarilyĤ. Check if they were ever paid by a medical device companyģ. tumor shredding devices spreading cancerĢ. defibrillators that were untested on humans Bayer committed fraud to claim customer/patient satisfaction with the Essure device Intuitive Surgical advised doctors to determine when they were ready to perform robotic surgeries on their own, intuitive surgical led Da Vinci training for doctors. Adverse effects aren’t known until years after it’s been on the market. Individual physicians don’t report adverse events typically. J&J was informed by the surgeons testing the mesh devices that it could cause all kinds of irreversible damage and chronic pain, but J&J ignored them and instead pushed their safety. Mesh devices could not be removed after implanted, increased scarring in surrounding tissue was like adding cement or bubble gum to your hair Essure was approved in 2002 by people ensuring the implants safety and efficacy who also had financial interest in its success (stock ownership, or who were paid endorsers) 510k procedure requirements are even less-restrictive than PMA and were authorized for medical devices to be fast-tracked to market. devices going through PMA (pre-market approval) only requires 1 study of the device with a minimum of twenty people
Why isn’t the FDA sufficiently testing implanted devices before putting them on market? How many people have been diagnosed with permanent disease that have reversible disease? ie: cobalt positioning causing psychosis and dementia like impairment Vaginal mesh devices (FDA did not require human studies) - flu like symptoms, infection, pain, other necessary surgery interventionsĭaVinci robot for a hysterectomy (FDA cleared it for less restrictive than PMA- 510k clearing requests) - vaginal cuff dehiscence, auto immune and systemic problems
Implants examined & other significant physical/neurological effects:ġ: Essure permanent birth control - significant bleeding, chronic inflammation and flu like symptoms, infection risk, systemic pain, chronic headache/migraines, chronic fatigue, auto-immune symptoms, faintingĢ: Metal on metal ASR hip replacement - doctor in documentary essentially had this implant liquify inside his body, cause cobalt poisoning, and cause symptoms of psychosis. This 100 minute documentary is a critical review of humanity’s first attempts of implanting medical devices inside the body.
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