If you are having any problems with your surgically
implanted vaginal mesh, please call me. 800-322-5543
Hi, I am Lynn Foley. As a registered nurse, attorney and woman I want to discuss a delicate,
Over the last several years, many women have undergone a procedure commonly known as
a bladder suspension or bladder sling for pelvic organ prolapse or stress urinary incontinence. Doctors surgically implant mesh within the pelvis
to provide support for the bladder and other female organs.
Unfortunately, many women develop side effects including: chronic pain, tissue damage,
infections, incontinence and other related dysfunctions, including pain during intimate relations. These problems compromise their quality of
life and may be permanent.
The mesh manufacturers failed to conduct proper testing and then failed to adequately
inform women of known side effects before they underwent the surgical procedure. As a result you may be entitled to money damages from the mesh
If you are having any problems with your sugically implanted vaginal mesh, please call
my office at: 800-322-5543
It is unacceptable
when a medical procedure intended to make a patient feel much better goes bad and causes additional pain and discomfort. Itís even worse if
the medical procedure causes serious, permanent debilitating injury or loss of life.
A good example is recent problems experienced with vaginal mesh, a good medical tool intended to restore a normal life to
women who have been suffering but sometimes results in their quality of life worsening.
Vaginal mesh has been commonly used by doctors for women suffering from pelvic organ prolapse where a womanís uterus, bladder
or rectum slips out of place. A common treatment has been to implant vaginal mesh to strengthen vaginal or other tissue that has weakened, usually
Surgical mesh, generally used to repair weakened or damaged tissue, is made from porous absorbable or non-absorbable synthetic
material or absorbable biologic material. Surgical mesh can be used for urogynecologic procedures, including repair of pelvic organ prolapse
and stress urinary incontinence. It is permanently implanted to reinforce the weakened vaginal wall for Pelvic Organ Prolapse (POP) repair or
support the urethra or bladder neck for the repair of Stress Urinary Incontinence (SUI).
About 100,000 women were treated for pelvic organ prolapse with surgical mesh in 2010, with 75,000 of those implanted vaginally.
The FDA for the first time began sending warnings to doctors, citing more than 1,000 manufacturer reports of complaints from 2005-2007. Since
then the number of complaints regarding vaginal mesh has increased five times. Most of the complications involve erosion where the skin breaks
and the device protrudes or contraction of the mesh that results in vaginal shrinkage.
Events regarding use of vaginal mesh have escalated rapidly since 2010. In 2012 the FDA ordered transvaginal manufacturers
to study the risks involved after receiving more than 3,800 reports in 2011 of complications related to vaginal mesh. As a result manufacturers
are required to submit study plans to the FDA that address specific safety and effectiveness concerns related to surgical mesh devices for pelvic
organ prolapse and single-incision mini-sling devices for incontinence issues. Data from the studies will enable the agency to better understand
the safety and effectiveness profiles of these devices.
Some of the dangerous side effects of vaginal mesh implants include
Erosion of the vaginal epithelium
Bladder of bowel perforation
Return of Pelvic Organ Prolapse
Because of the growing reports of complications, there has been a marked increase in lawsuits filed against manufacturers
Ė as of May 2012, 335 against AMS, 268 against Johnson & Johnsonís Ethicon division, 205 against Boston Scientific and 645 lawsuits filed
against C.R. Bard.
In March 2012 Bloomberg News reported that Johnson & Johnson sold vaginal mesh implants for three years before was approved
for use by the FDA.
Because of these developments, any woman who has had a vaginal mesh implant should make an appointment with the physician
who performed the implant for an examination and to learn from the doctor which manufacturer made the device. After having all their medical
questions answered, afflicted women should then talk with a knowledgeable attorney about what actions, if any, should be taken. To succeed in
a product liability claim the patientís well-being has to be made worse because of a treatment or procedure, the worsened condition has
to be the result of negligence, and it certainly helps when there has been a willful decision to continue after warnings have been issued.
Manufacturers will and have ignored warnings and cautions from the FDA but they do listen closely to their attorneys when
advised of the filing of product liability claims. Any woman who has been harmed by a vaginal implant should consider legal action as a
means to stop manufacturers continuing business practices that will harm other women. Victims of vaginal implants should also consider legal
action as a means of getting the justice they so much deserve.
So my best advice to vaginal mesh implant victims is to first consult your physician and then consult an attorney who specializes
in medical equipment malfunctioning. This is the very best way to make a painful situation better and find a remedy for women who become victims
because of the greed and carelessness of people and companies they should be able to trust.
About the Author: Lynn M. Foley is a senior partner in the Law Offices of Cochran, Foley & Associates, of Livonia, Michigan.
Foley, also trained as a Registered Nurse, specializes in medical malpractice cases. Video interview with Lynn Foley
Cochran, Foley & Associates, PC, is a Michigan law firm specializing in medical malpractice, personal liability, and
SSD/SSI appeals that does not represent insurance companies or corporations but instead bases its fees upon representing individuals and families.
Cochran, Foley Associates won $15.8 Million, the largest award in Michigan for a medical
malpractice case. If you had a vaginal mesh implant and believe it is faulty call us at 800-322-5543 for a free consultation.