On this page, we'll discuss an overview of the Transvaginal Mesh Recall, the status of Transvaginal Mesh Lawsuits, issues surrounding transvaginal mesh...
Medical device makers such as C.R. Bard and Ethicon have issued a transvaginal mesh recall for device models that have been linked with serious injuries.
Despite thousands of reports of serious injuries, there's been only one transvaginal mesh recall. Though, several companies have discontinued their devices.
Complications of surgical mesh for transvaginal pelvic organ prolapse repair are “not rare,” says the FDA. Issues range from pain to vaginal tissue erosion.
Transvaginal mesh is a net-like implant for stress urinary incontinence (SUI) and pelvic organ prolapse (POP). Supports weakened vaginal wall or bladder neck.
Blood Pressure Monitor Lawsuit Alleges Omron Platinum Readings Are ‘Wildly Inaccurate’ ; Bard Loses Appeal, Set to Pay $2 Million in Mesh Verdict ; FDA Reclassifies Transvaginal Mesh as a High-Risk Device
FDA Orders Mesh Manufacturers to Stop Selling Devices for Transvaginal Repair of Pelvic Organ Prolapse ; On April 16, 2019, after reviewing their premarket approval (PMA) applications, the FDA ordered all manufacturers of surgical mesh intended for transvaginal repair of pelvic organ prolapse (Boston Scientific Uphold Lite, Boston Scientific Xenform, Coloplast Direct Fix Anterior) to stop selling and distributing their products immediately. The FDA determined that the manufacturers, Boston Scien...
Update to Mesh Hub notifying of recent recall actions
Revision surgery is a surgery to remove or repair transvaginal mesh. Women who suffer problems from transvaginal mesh may need multiple revision surgeries.
Some of the medical device liability cases we focus on include: Adult Palate Expanders · Breast Implants (BIA-ALCL) · Exactech Knee, Ankle, & Hip Replacements · Hernia Mesh · Implantable Ports · Paragard · Transvaginal Mesh · Surgical Staplers · Synovo Total Hip System · Zimmer Biomet CPT Hip System