Vaginal Mesh Lawsuit News: Carey Danis & Lowe Transvaginal Mesh Lawyers Remark on Growing Ethicon MDL 2327

As a defective medical device law firm representing individuals who claim to have been injured by defective medical devices, such as Ethicon's vaginal mesh product, the Gynecare Prolift, Carey Danis & Lowe transvaginal mesh lawyers remark on the continually growing Ethicon MDL 2327. Carey Danis & Lowe continues to investigate transvaginal mesh lawsuits, as more and more individuals approach the law firm with new claims citing injury from transvaginal mesh.

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Vaginal Mesh Lawyers at Carey Danis & Lowe

Carey Danis & Lowe Vaginal Mesh Lawyers

For more information about vaginal mesh products, such as Ethicon's Gynecare Prolift, vaginal mesh lawsuits, and the Ethicon MDL, contact a Carey Danis & Lowe transvaginal mesh lawyer today by calling 800-721-2519.

St. Louis, Missouri (PRWEB) May 30, 2013

Carey Danis & Lowe transvaginal mesh lawyers have been closely following the Ethicon multidistrict litigation (MDL) in the U.S. District Court for the Southern District of West Virginia. The case is In re: Ethicon Inc., Pelvic Repair System Products Liability Litigation MDL No. 2327. Carey Danis & Lowe continues to monitor the Ethicon MDL as they are a law firm that represents individuals who allege to have been injured by Ethicon's Gynecare Prolift vaginal mesh product.

As of May 28, 2013, there were 6,607 vaginal mesh lawsuits filed against Ethicon in the Ethicon MDL, according to the U.S. District Court's case list.* As new lawsuits appear to have been continually added to the Ethicon MDL, with 39 vaginal mesh lawsuits consolidated into the Ethicon MDL on May 23, 2013, transvaginal mesh lawyers at Carey Danis & Lowe also continue to receive new claims citing injury from the Ethicon Gynecare Prolift.

As a result of the growing number of claims being received by Carey Danis & Lowe transvaginal mesh lawyers, the St. Louis based law firm will continue to provide individuals who claim injury from vaginal mesh with free legal consultations. In addition to free legal evaluations, Carey Danis & Lowe has developed a vaginal mesh information page that is intended to be an invaluable resource for individuals seeking to learn more about vaginal mesh products and vaginal mesh lawsuits.

While Carey Danis & Lowe further investigates new vaginal mesh claims, the U.S. Food and Drug Administration (FDA) is also currently conducting a review of vaginal mesh as it relates to pelvic organ prolapse (POP) surgery and stress urinary incontinence (SUI) surgery. Thus far, the FDA has identified vaginal mesh erosion as the most common complication reported in individuals who have received a vaginal mesh implant. The FDA has also cited vaginal mesh contraction as another complication reported by individuals submitting adverse event reports.**

For more information about vaginal mesh products, such as Ethicon's Gynecare Prolift, vaginal mesh lawsuits, and the Ethicon MDL, contact a Carey Danis & Lowe transvaginal mesh lawyer today by calling 800-721-2519.

About Carey Danis & Lowe

Carey Danis & Lowe is a plaintiff's litigation firm based in St. Louis, Missouri with law offices across the United States in Illinois, Missouri, and Florida. Carey Danis & Lowe specializes in defective drug and pharmaceutical litigation and class action lawsuits. The Carey Danis & Lowe team is comprised of experienced attorneys working alongside knowledgeable professional staff that includes medical doctors, nurses, and information technology specialists. Contact Carey Danis & Lowe at 800-721-2519.

Sources

** U.S. Food and Drug Administration Vaginal Mesh Safety Communication: http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm262435.htm


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