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Vaginal Mesh, Another Device Harming Women, Vaginal Mesh Lawsuit Lawyers

Written by lisaspitzer on . Posted in Alabama Yaz lawyer, Alaska Yaz Lawyer, Arizona Yaz Lawyer, Arkansas Yaz Lawsuit, California Yaz Attorney, Delaware-Yaz-Lawsuit, Florida Yaz Lawyers, Georgia Yaz Lawyers, Hawaii Yaz Lawyers, Idaho yaz Lawsuit, Illinois Yaz Lawyer, Indiana Yaz Lawyer, Iowa Yaz lawyers, Kansas Yaz lawsuits, Maine Yaz Lawyer, Maryland Yaz Lawyer, Massachusetts Yaz lawyers, Michigan Yaz Lawyers, Minnesota yaz Lawyers, Mississippi yaz lawyer, Missouri yaz lawyer, Montana yaz Lawsuit, Nebraska yaz lawyer, Nevada Yaz lawyer, New Hampshire, New Jersey, New York, North Dakota, Oklahoma-yaz-Lawyer, Oregon-yaz-Lawyers, Pennsylvania yaz Lawyers, Rhode Island, Yaz Lawyer Colorado, Yaz Lawyer Connecticut

Vaginal Mesh Helpline www.vaginalmeshhelpline.com is helping women injured by the Vaginal Prolene mesh. The vaginal mesh lawsuits have begun and just like Yaz this is a device harming 1000's of women. Manufacturers love to target women and the elderly.

Vaginal Mesh Helpline 1 877 522-2123 Vaginal Mesh Lawyer   Vaginal Mesh, Bladder Sling, Transvaginal Mesh Lawyer

Experienced Vaginal Mesh lawsuit lawyers to file your mesh lawsuit. Vaginal Mesh Helpline 1 877 522-2123 Speak to a female Social Worker about your mesh lawsuit. Choose your lawyer carefully vaginalmeshhelpline.com
1 877 522-2123 Polypropylene Knitted Mesh (PPKM) fabrics are comprised of monofilament yarns, which are engineered for the manufacturing of textile fabrics. The polymer and manufacturing processes that are used produce fabrics with properties that are used in the manufacturing of medical devices including hernia mesh patches, stress urinary incontinence (SUI) slings, and vaginal prolapse suspenders or known as the The Vaginal Mesh.
Problems with polypropylene fabrics have led to warnings being issued for various products made from nonwoven material and in some cases, the manufacturers have stopped marketing the products

According to adverse reports submitted to the FDA from nine different manufacturers, more than 1,000 people have suffered severe complications from surgical mesh implants. The reports include infection, pain, urinary problems and bowel, bladder or blood-vessel perforations. The repaired prolapse may have recurred or incontinence increased. Additional surgeries to remove mesh have been required because of vaginal erosion.

Transvaginal Surgical Mesh to Treat SUI

Sudden Urinary Incontinence (SUI) is estimated to affect as many as 11 million women in the United States. It is generally defined as the sudden, involuntary loss of urine when a patient is laughing, sneezing, coughing or exercising. SUI is caused by anything that may have led to serious pelvic muscle strain or weakness such as vaginal childbirth. It can be exacerbated by estrogen and other hormonal imbalance accompanying menopause. This has a huge effect on our baby boomer population.

Nearly 40% of all adult American women will experience various degrees of SUI during their lifetime. Symptoms can range from occasional leakage of a few drops of urine to complete loss of urine under certain conditions of stress. Although nonsurgical methods such as dietary changes, bladder retraining, Kegel exercises, biofeedback, pessaries,and drug therapies have been used successfully to treat these women, many patients eventually require surgical repair to relieve their symptoms.

Transvaginal Surgical Mesh to Treat POP vaginalmeshhelpline.com

The problem of incontinence for women from various causes becomes more common after pregnancy and in menopause, when surgery can be recommended after other non-intrusive treatments are not found effective.

These conditions are referred to as Pelvic Organ Prolapse (POP).

POP is the term that describes a condition when a pelvic organ drops from its normal location and pushes against the walls of the vagina. This generally occurs when muscles that hold pelvic organs in place are weakened or stretched by childbirth or surgery. POP can lead to symptoms that include pain, discomfort, loss of bladder control and constipation, infection, organ perforation and painful sexual intercourse .
One popular product, known as the transobturator vaginal sling, was made by Mentor Corporation. This product was more commonly called “OB Tape.”

Mentor manufactured an OB Tape vaginal sling that was not recalled, but the company stopped marketing it in the spring of 2006. The product used a nonwoven material which made it different in design than most other mesh devices. The nonwoven fabric is alleged to have blocked oxygen and nutrients, substantially increasing the risk of problems such as infection. This impedance potentially can cause serious problems with the device that may not appear for months, or even years following implantation surgery.

If you have had this surgery and are experiencing symptoms immediately contact your health care provider.
Vaginal Lawyer Network lawyers are filing mesh lawsuits to protect women.

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