Here are the details on Essure... read this especially if you are
considering having this done...
Washington D.C., Dec 31, 2015 / 05:35 pm
(CNA).- Perforated organs, metal coils lodged in colons, fetal
disfigurement due to nickel poisoning. Chronic pain, exhaustion, bouts of
depression and suicidal thoughts.
It's the stuff nightmares are made of. But these are real symptoms that
are being blamed on a real medical device, one that is being protected by
the FDA. The device, Essure, is a permanent type of birth control in the
form of tiny metal coils inserted into women's fallopian tubes.
But while it's been on the market since 2002 and has been touted as safe
and effective, thousands of people are starting to come forward and
question the device, including doctors very familiar with it.
It started out as a standard procedure for Dr. Shawn Tassone, Ob/Gyn. He
was inserting Essure coils into a patient. The 10 minute, in-office
procedure was supposed to be quick, simple and painless, and it was one he
had performed many times before.
"I remember…I put the Essure in, exactly like how you were supposed to,
and then as I sat there the tube started to spasm, and it pulled the
Essure in," he told CNA. "It disappeared, it coiled right into the tube."
Unsure of how to proceed, he looked at the product manufacturer's
representative, who was in the room with him. The representative told him
to just put another coil in the same tube, but Dr. Tassone knew that was
against the product's instructions.
"I told (the representative) that, and he was like, 'Nah, that's not
necessarily true'," Dr. Tassone said. "And you're just being told this
stuff by these reps who are college graduates, and I'm sure their hearts
are in the right place, but they also want you to do the procedure because
they get reimbursed more."
It was through personal experiences with patients, as well as hearing
other women's stories, that Dr. Tassone eventually stopped doing a
procedure he'd once been so sure was safe and effective. He said that
while he's not a conspiracy theorist, he does believe there are a large
number of women with severe complications from Essure that are not being
acknowledged by the medical community at large.
A Facebook group 24,000 strong
A lot of these women can be found on the Facebook group, Essure Problems.
Of the 24,000-plus members, the majority are women who share a strange
kind of sisterly bond – almost all of them have had Essure, and almost all
of them bitterly regret it.
When the Essure coils are implanted, they are supposed to stay in the
fallopian tubes, where they create a chronic infection that will cause
scar tissue to form around the coils, effectively closing the tubes and
rendering the woman sterile. The device was first manufactured by the
group Conceptus and pre-approved by the FDA before hitting the markets in
2002. In June 2014, Conceptus was bought by Bayer, which has continued to
manufacture and distribute Essure.
Some possible side effects after the Essure insertion procedure are listed
on the product's website and include: "mild to moderate pain and/or
cramping, vaginal bleeding, and pelvic or back discomfort for a few days.
Some women experienced nausea and/or vomiting or fainting. In rare
instances, an Essure insert may be expelled from the body."
Angela Desa-Lynch, an administrator for the Essure Problems group, said
the women in the group have experienced these problems to the extreme.
"Whatever they've put on the label, multiply it by 200," she said. "They
say chronic pain, or they say mild cramping or abdomen pain, but they
don't tell you that it's debilitating. They don't tell you that it's 'I
can't get out of bed and take care of my kids' kind of pain."
When Desa-Lynch had her Essure coils in, she said she felt like she had
the flu constantly. She was 28 years old, and her youngest son was just
three months old.
"My little son…he had no idea the real parent I could be, because I was
going through all these health problems," she said. Desa-Lynch had to have
a total hysterectomy to remove the coils, but she said the recovery
process didn't end with the removal.
"You're mad," she said. "This is not what I signed up for. I just wanted a
birth control, I didn't want a life time of health issues, and to remove
my woman parts, that's not ok."
Watching the posts on the page can be an emotional rollercoaster, Desa-Lynch
said. She hears from women who've become depressed, suicidal, divorced,
bankrupt, or a combination of those things after having complications from
Moving coils and the difficulty of removal
One of the most horrific complications is device migration, where the coil
leaves the tube and becomes lodged in other parts of the body, usually the
colon or somewhere in the pelvis. This can cause a blocked colon or other
It can be extremely difficult for women who want to have their Essure
coils removed. Many doctors will deny that the Essure is the root of
women's problems, because the clinical trials they've seen from the FDA
claim the risks of such complications are so low.
Additionally, Medicare and most insurance companies classify Essure
removal as "cosmetic," which further disincentivizes doctors to remove the
coils and often puts women who require the removal into personal debt.
"One woman had a coil in her colon, she went from a business owner to
bankruptcy" after four surgeries to remove it, Desa-Lynch said.
Physical removal of the coils can also be difficult because they are
fragile and may break.
"You have fragments now in your body, and we've had women where they come
back after removal and they have these masses growing in their abdomen,"
Desa-Lynch said. "Your body's going to try to encapsulate whatever foreign
object is there, and now you have all these little cysts growing
Both she and Dr. Tassone said that from what they've seen, the only
completely safe and secure way to make sure all of Essure is removed is a
What happens if you get pregnant with Essure?
Then there are the women who become pregnant while using Essure. No
sterilization method is guaranteed to work 100 percent of the time, save
for a total hysterectomy with removal of the fallopian tubes. According to
Essure's website, the device is 99 percent effective at preventing
pregnancy, but that is with so-called perfect use.
In the real world, doctors may misplace coils or a woman's tubes can heal
or push Essure out. Furthermore, women given Essure are told to use an
alternative form of contraception for the first three months following the
procedure until a second appointment which checks for proper coil
placement – but many women fail to follow through on this step.
Given these margins for error, a recent Yale School of Medicine study
estimated 96 of every 1,000 women who undergo hysteroscopic sterilization,
or Essure, would get pregnant within 10 years. For laparoscopic tubal
ligations (known as 'having your tubes tied'), the pregnancy risks were
significantly lower: 24 to 30 pregnancies per 1,000 women.
In an e-mail interview, FDA representative Eric Pahon told CNA that
clinical trials of women who became pregnant with Essure showed "no
increased risk of neonatal or pregnancy complications, as long as the
pregnancy is in the uterus. The FDA will continue to monitor the safety of
Essure to make certain."
What the women of Essure Problems have found is that doctors will not
remove the coils even if a woman becomes pregnant. Most will automatically
recommend abortion, because they don't know what to do.
"They don't know what can happen, because there is nickel in Essure and it
can leach, and the device can move and perforate the sack and has done it,
so because the doctors don't know how to treat you, that's the first thing
they ask you to do is to terminate," Desa-Lynch said.
Should a woman with Essure choose to continue the pregnancy – and many of
them do – she risks nickel poisoning and device migration to her baby, and
a 55 percent chance of miscarriage, according to the numbers from the
"Your baby isn't growing"
One Essure pregnancy story stood out to Desa-Lynch as particularly
jarring. A young woman in the Facebook group, born and raised as a devout
Catholic, became pregnant despite being on Essure. At 24 weeks of
pregnancy, the doctors told her: "Your baby is not growing."
Her baby had gotten nickel poisoning, so the brain wasn't developing and
the limbs weren't growing properly. The young woman was told her baby at
best would be severely deformed at birth, if not completely brain dead.
"When you're Catholic, abortion is not something that crosses your mind,
you just think 'ok, well, we'll deal with this'," Desa-Lynch said.
However, after the grim diagnosis, the young woman chose abortion. Desa-Lynch
said the woman doesn't even comment on the Facebook page because she is so
haunted by her experience, but she's there, and she watches the comments.
"I can't imagine being in her position," Desa-Lynch said. "It puts you in
a hard spot. Here you think you're doing what's right for you, what's
right for your family, and what's right for your health, and now you're
facing these situations that you don't even know how to handle and neither
does your doctor, and you have to go against all of your morals and
values…I don't know what I would do."
"It goes against a lot of women's morals," she added, "and women get
severely depressed. Someone posted just yesterday that one of her good
friend's daughters had (Essure) put in and she killed herself, because
they go to a doctor and they don't listen to you."
When the suicidal posts started popping up more frequently, the group
administrators decided to set up a buddy system of sorts. They connected
women in the group with other women who were close by, so that they'd
always have someone they could go to who understood their situation. The
administrators watch posts closely and alert the smaller state groups of
"We work collectively and united," Desa-Lynch said. "It's amazing to see
women pull together the way that they have and fight for each other."
False data and bad numbers
As a medical device, Essure had a questionable start at best. When it was
pre-approved by the FDA in 2002, the FDA used clinical trials from the
device manufacturer, the company which would profit from the approval and
sales of the device, to determine whether or not it was safe for women.
When asked if this process created a conflict of interest, the FDA
responded: "Although the manufacturer may submit any form of evidence to
the FDA in an attempt to substantiate the safety and effectiveness of a
device, the FDA relies upon only valid scientific evidence to determine
whether there is reasonable assurance that the device is safe and
Desa-Lynch and the administrators of Essure Problems have three full sets
of records from the clinical trials that show complaints of abdomen pain
in women in the trial being marked off as "unrelated."
Dr. Tassone has seen the clinical trials, and said there are times when
the ages of women with complaints or complications are crossed off and
altered in order to better fit the picture the manufacturer wanted to
"The clinical trials that they were basing their information on were
falsified, and we've brought this to the FDA," Desa-Lynch said. "They (the
FDA) just say, 'upon their investigation they find everything to be safe,
they find the benefits to outweigh the risks'."
In addition, it is basically impossible to track exactly what percentage
of women with Essure have experienced severe complications. Although Bayer
and the FDA know that 750,000 kits have been sold, there's no one keeping
track of how many women have had the procedure.
Further complicating the numbers is the fact that multiple kits can be
used for a single procedure. Dr. Tassone said he's used up to three kits
on a single woman, which happens if coils break before or during
"We have over 200 women who've had two kits used on them," said Desa-Lynch
of the Essure Problems group, "So it's kind of hard to give a percentage
on bad numbers."
Protected status and incentives
But despite the thousands of complaints, Essure is classified as a Class
III medical device, a category reserved for devices with PMA (premarket
approval). These devices are pre-empted, which means people injured by the
product cannot collect damages from the manufacturer.
Typically, Class III medical devices are live-saving devices such as heart
stints. The idea behind preemption is that by protecting companies from
having to pay damages, it encourages them to continue creating better
devices that are necessary for saving and sustaining lives.
The only Class III, protected medical devices that do not save or sustain
life? Essure coils and breast implants.
"This is part of the problem," Dr. Tassone explained. "When you are having
studies being done by companies who are falling apart (Conceptus was
bought out by Bayer), you have an inherent bias. If the (product) is
revoked, then this multi-million dollar project was flawed somehow and
they lose money."
"And you see that with other devices, there is a lot of money involved,
and the FDA is not doing due diligence, because sometimes the FDA has
people on it who are not necessarily getting paid, but who are affiliated
with some of the big companies."
Doctors, too, receive incentives for using Essure. If they meet a certain
implantation quota, the manufacturer gives them a $20,000 scope that can
be used to perform multiple procedures. Doctors also are often paid to
attend Essure trainings and conferences.
But Dr. Tassone said he believes that most doctors originally implanted
Essure because they were told, and truly believed, it was a safe and
"We were told in the beginning that it doesn't cause any pain and the
initial studies that came out said that," he said. "It makes it look like
the doctors are getting greedy by putting Essure in because we get more
money, but in reality, 99 percent of us actually believed it was a good
procedure and was safer for the patients and it worked."
He said the procedure itself is still considered less risky than a tubal
ligation, which is an involved surgery rather than an in-office procedure.
Still, Dr. Tassone stopped implanting Essure about a year and a half ago,
and he said it usually doesn't take much to convince his patients to opt
for a different procedure.
"The way I counsel my patients now, I send them to what the Facebook group
says," he explained. "Usually I tell them Essure is a foreign body and
it's permanent - most women don't want that, when you explain it that
Lawsuits and Erin Brockovich
There are only a few pending lawsuits involving Essure at the moment, Desa-Lynch
said, because the PMA act goes all the way up to Congress.
But the Essure Problems Facebook group intends to fight until Essure is
off the market and the PMA act is changed. And they just might win,
because of a certain famous legal clerk and environmental activist that
has joined their fight.
"It kind of started as a joke on the form, like, 'Let's e-mail Erin
Brockovich, haha'," Desa-Lynch said. But they did, "and she listened!"
Made famous from a 2000 film about her life as a single mother and
environmental activist, Brockovich has created a website, http://www.essureprocedure.net/,
where women who've had Essure can share their stories and where she posts
the latest news about the fight against the device.
"That right there kicked off the empowerment, that kicked off the movement
of 'Ok, we can do this'," Desa-Lynch said.
Dr. Tassone said he'd like to see more acknowledgement from the medical
community of the pain and suffering Essure is causing some women, as well
as more transparency from the manufacturers.
"Acknowledgement is the first step," he said. "Like the company saying,
'Yeah, this is a foreign body and okay, let's take a look at this.' That
would go a million miles for some of these people, that maybe, it's not
all just in their head."
He also wonders whether a device that caused similar reactions in men
would even be on the market.
"If you have a coil and you said you were going to use it in men for
vasectomies and you were going to insert it in to block the testicle from
having sperm come out, would we be doing that or not? Because they could
feel that implant," he said.
"But with tubes, and in women's health – because everything is on the
inside - I think it's out of sight, out of mind."
Until the Essure Problems group can get their case pushed through in
court, Desa-Lynch said it's enough for them to keep informing women and to
prevent them from getting Essure.
"We've saved over 600!" Desa-Lynch said proudly. "We keep track of them.
That right there is enough to know that this is the right thing to do."
Update: In June 2015, the FDA updated and expanded the risks associated
with the device listed on the Essure product packaging. In September 2015,
the FDA met with representatives of the "Essure Problems" women, and later
announced that they will be releasing a new safety review of the product
in February 2016. In November 2015, U.S. Representative Mike Fitzpatrick
(R-PA) introduced a bi-partisan bill called the "E-Free act" to Congress
that would pull the device from the market and put additional pressure on
An earlier version of this article was originally published on CNA Feb.