Ohio Medical Device Lawyer Reviewing Defective Transvaginal Mesh Implants for injured plaintiffs nationwide
A transvaginal mesh implant, also known as pelvic mesh, is a type of medical device that is used to treat two common medical conditions: Pelvic Organ Prolapse and Stress Urinary Incontinence. These conditions may occur following child birth and pregnancy.
UPDATE: The FDA has discontinued the sales and use of some pelvic mesh devices for the reparation of pelvic organ prolapse due to injury risk.
More than 1000 reports of mesh complications with defective transvaginal mesh implants referenced in the FDA notification raised concerns about the adequacy of training, and the ability to prevent complications. In February 2009, the FDA advised clinicians using transvaginal mesh implants for pelvic organ prolapse and stress urinary incontinence that the clinicians should: (1) obtain specialized training, (2) be aware of adverse events associated with a transvaginal mesh implant, (3) inform patients of risks and treatment options, and (4) provide patients with the product labeling. Since this warning, thousands of women have brought product liability actions for injuries arising from the use of defective transvaginal mesh.
Joe Lyon is a highly-rated Cincinnati recall lawyer and Ohio medical device lawyer representing plaintiffs throughout the United States who have been injured by transvaginal mesh implants.
If you have questions whether in injury was caused by a defective transvaginal mesh implant or the state of the national medical device litigation, please call for a free and confidential consultation.
Transvaginal Mesh Implant Injuries
The complications and side effects possibly related to defects in the pelvic mesh. The side effects include:
- erosion of the vaginal epithelium
- serious infection
- recurrence of the pelvic organ prolapse
- urinary incontinence
- pain during intercourse
- severe bleeding
- bladder perforations
- pelvic hemorrhage
- bowel perforation
- blood vessel perforation
- vaginal scaring
- mesh erosion
Transvaginal Mesh Implant Complications
- Revision surgery to trim the transvaginal mesh implant
- Revision surgery to remove the transvaginal mesh implant
- Physical therapy
- IV therapy
- Surgical repair of damages organs
Transvaginal Mesh Defect Lawsuits
The Lyon Firm cannot offer medical advice, but the medical literature has recommended the following regarding pelvic mesh implants:
- patients should be informed that the use of mesh for pelvic floor repairs is considered a “novel technique”;
- patients should be informed on the range of successes;
- physicians should undergo specific training for these operations;
- preoperative counseling should include a discussion of the adverse events that include—mesh exposure, pain, and dyspareunia;
- trocarless kits are considered investigative.
Vaginal Mesh Implant Injury
The guidelines further stated that the following factors may increase the adverse events:
- lack of full thickness dissection
- improper mesh placement
- estrogen status
- patient nutritional status
- inadequate hemostasis
Transvaginal Mesh Implant Safety Warnings
Although the products are widely used, there is little science comparing the pelvic mesh procedures to traditional surgical methods.
Altman conducted a randomized, controlled trial comparing the use of a standardized trocar guided mesh kit with the traditional anterior colporrhaphy surgery. The trial was limited to 389 women and the composite was based on both a subjective and objective outcome. While there was a lower rate of recurrence of pelvic organ prolapse after one year, there was a higher rate of adverse events, including bladder perforations, pelvic hemorrhage and mesh related complications. “[The] results highlight the need for careful evaluation of surgical innovations, which are often widely adopted in the absence of data from clinical trials.”
Defective Pelvic Mesh Devices
In light of the ongoing litigation in West Virginia and New Jersey, as well as the ongoing FDA investigation, Johnson & Johnson informed both the State and Federal Courts yesterday by way of formal letter, that it intends to “discontinue or revise, as appropriate, all marketing materials” and to stop worldwide sales of the following devices:
- Gyencare TVT Secure
- Gynecare Prosima, Pelvic Floor Repair System
- Gynecare Prolift, Pelvic Floor Repair System
- Gynecare Prolift +M, Pelvic Floor Repair System
Transvaginal Mesh Defects & Safety
In January, the FDA ordered that J&J and 30 other makers of vaginal mesh implants implement studies to assess organ damage and other health complications alleged to be related to the products. The FDA further reported in March that The Gynecare Prolift has been sold for three years without proper regulatory approval.1
Defective Transvaginal Mesh Implant Lawyer
The Lyon Firm files product liability lawsuits against medical device companies when defective medical devices cause injury to patients, requiring revision surgery and painful after effects.
If you or a loved one has suffered an injury due to faulty transvaginal mesh implants and have questions about the root cause and the legal remedies available to improve quality of life and medical care in Ohio, contact The Lyon Firm at (800) 513-2403. You will speak directly with Mr. Lyon, and he will help plaintiffs answer critical questions regarding defective vaginal mesh lawsuits.