Contact Us

Transvaginal Mesh Injury
*    Denotes required field.

   * First Name 

   * Last Name 

   * Email 


Cell Phone 

Street Address 

Zip Code 



Transvaginal Mesh Manufacturer / Model

Please describe any problems or injuries caused by the Transvaginal Mesh

For verification purposes, please answer the below question:

No Yes, I agree to the Parker Waichman LLP disclaimers. Click here to review.

Yes, I would like to receive the Parker Waichman LLP monthly newsletter, InjuryAlert.

please do not fill out the field below.

New MDL Established for Coloplast Transvaginal Mesh Lawsuits

Aug 24, 2012 | Parker Waichman LLP

Transvaginal mesh lawsuits continue to pile up, resulting in yet another multidistrict litigation (MDL) being established in West Virginia federal court.  Lawsuits alleging injuries from Coloplast transvaginal mesh and pelvic sling products have been transferred to U.S. Judge Joseph Goodwin in U.S. District Court, Southern District of West Virginia.  Judge Goodwin is already overseeing four other transvaginal mesh litigations, involving products made by C.R. Bard, Johnson & Johnson/Ethicon, Inc., American Medical Systems, Inc., and Boston Scientific Corp.

So far, 24 lawsuits are pending in the new Coloplast transvaginal mesh MDL.  MDLs are established when a large number of lawsuits associated with a particular product have been filed.   The complaints are coordinated under one judge for pretrial litigation to avoid duplicative discovery, inconsistent rulings and to conserve the resources of the parties, witnesses and the court. When lawsuits are consolidated as a multidistrict litigation, each retains its own identity. If the multidistrict litigation process does not resolve the cases, they are transferred back to the court where they originated for trial.

Like similar devices, transvaginal mesh products made by Coloplast are used to treat pelvic organ prolapse and stress urinary incontinence.  The safety of transvaginal mesh devices is under scrutiny, as the have been the subject of thousands of reports of serious injuries, including:

•    Inflammation and infection
•    Pain from mesh shrinkage
•    Extrusion of mesh through the vaginal wall
•    Pain during intercourse and urination

The U.S. Food & Drug Administration (FDA), which has been studying the safety of transvaginal mesh since 2008, recently asked transvaginal mesh manufacturers to conduct post-market safety studies of their products. The agency is considering moving transvaginal mesh for pelvic organ prolapse repair to a higher risk medical device category.

Parker Waichman Accolades And Reviews Best Lawyers Find Us On Avvo