News and Articles

Rottenstein Law Group Hopes Congress Collects Documents To Determine When Surgical Mesh Manufacturers First Learned of the Safety Issues Associated With Their Product

The Rottenstein Law Group, which represents clients with claims stemming from the adverse effects of vaginal mesh, hopes the U.S. House of Representatives\' Committee on Energy and Commerce holds \"hearings to examine whether FDA device regulation has been ineffective in protecting the public from dangerous medical devices like the Lap-Band and intravaginal mesh\" and that the committee seeks \"documents from the manufacturers of surgical mesh to ascertain when they first learned of the safety issues associated with certain uses of the device and what, if any, actions [the manufacturers] took to limit risks for patients.\"

Bill Would Block FDA 510(k) Approval For Medical Devices Associated With Recalls

Bernstein Liebhard reports on a newly introduced bill that would prevent medical device manufacturers from using the 510(k) process to receive FDA approval if they are predicated on previously recalled products.

New Lawsuit Filed Blaming DVT on NuvaRing: AttorneyOne.com Provides Advice and Solutions for the Alleged Side Effects from NuvaRing

According to court documents, in a suit filed on Jan. 9 in the Eastern District of Texas, Sherman Division, no. 4:12-cv-00008, a Danton woman, Dawn Kregel, used the NuvaRing for just over a month in 2010. NuvaRing is a contraceptive in vaginal ring form. Kregel accuses the company manufacturing NuvaRing in a $10 million lawsuit stating she was diagnosed with a DVT, allegedly caused by the defendants\' products. Now, AttorneyOne.com, a recognized authority on law, can provide helpful, proven advice and simple solutions including how to get in contact with so anyone can easily and inexpensively deal with cases of NuvaRing side effects.

House Democrats Call for Safety Hearings on Lap Bands and Transvaginal Mesh

Ennis & Ennis, P.A. Supports the House Democrat’s Position in Questioning Whether FDA Medical Device Approval Process Protects the Public

Innovative Product Improves Chances of Conception

It may be surprising to know that 10% of Canadian couples have a difficult time conceiving. By age 30, experts say, a woman\'s chance of conceiving each month is about 20%, and by the time she reaches the age of 40, it drops to 5%. A new product, called Zestica Fertility, recently approved by Health Canada, is now available to help couples increase their chances of conceiving.

New Lubricant Designed to Help Couples Get Pregnant

For many couples, rather than being an enjoyable experience, trying to get pregnant can actually become a stressful and even a depressing experience. This is especially true when conception does not occur within the first year of trying. A new product, called Zestica Fertility, recently approved by Health Canada, is now available to help couples increase their chances of conceiving.

Rise in Elective C-Sections May Increase Risk of Surgical Adhesions in Moms

With the number of women having cesarean sections on the rise, the risk of post-operative abdominal scar tissue, or adhesions, among mothers may also be increasing. Adhesion Related Disorder activist Karen Steward today joined the call for obstetricians to consider the risk of adhesion-related complications when recommending cesarean versus vaginal delivery.

Rise in Elective C-Sections May Increase Risk of Surgical Adhesions in Moms

EurekaMag.com Publishes New Reviews of Aurora Borealis, Bayam and Uterus Didelphys

The geographical and health sciences website EurekaMag.com publishes insights into specific subjects of all areas of geographical and health science. The latest reviews cover Aurora borealis which are the Northern Lights caused by radiation emitted as light from atoms in the upper atmosphere as they are hit by fast-moving electrons and protons, and bayam which is amaranth, a herb with approximately 60 species and inflorescences and foliage ranging from purple to red and gold. The latest insight into Uterus didelphys is about a uterine malformation where the uterus is present as a paired organ as the embryogenetic fusion of the mullerian ducts failed to occur.

FDA Orders Companies to Examine Complication Rates of Transvaginal Mesh Implants: AttorneyOne Notes Adverse Events Reports Are Increasing

Earlier this month, the FDA probed major companies on transvaginal mesh risk. Transvaginal surgical mesh is used to treat pelvic organ prolapse (POP) and Stress Urinary Incontinence (SUI). Lawsuits have been filed against C.R. Bard, the manufacturer of Bard Avaulta mesh, alleging the Bard Avaulta System is defective. The Bard Avaulta litigation was consolidated in October 2010 as part of an MDL (No.2187) in the US District Court for the Southern District of West Virginia. On January 26, the U.S. Judicial Panel on Multidistrict Litigation (JPML) will hear arguments over whether several transvaginal mesh lawsuits involving other manufacturers should also be centralized as part of three separate for coordinated handling. Now, AttorneyOne.com, a recognized authority on law, can provide helpful, proven advice and simple solutions including how to get in contact with legal council so anyone can easily and inexpensively deal with cases of transvaginal surgical mesh complications.

FDA Requires Transvaginal Mesh Makers to Study Risks

Ennis & Ennis, P.A. explains the FDA’s Order to manufacturers of transvaginal mesh devices requiring safety studies to be conducted on the devices used to treat pelvic organ prolapse and stress urinary incontinence.

FDA Requires Transvaginal Mesh Makers to Study Risks

Femanol, Vaginal Odors Worst Enemy, Celebrates Five Year Anniversary

MedcoSouth Healthcare LLC announces the five year anniversary of its ground breaking product, Femanol.

FDA Requires Transvaginal Mesh Makers To Conduct Safety Studies

Bernstein Liebhard LLP endorses an FDA mandate requiring transvaginal mesh manufacturers to initiate investigations into implant related injuries.

Rottenstein Law Group Launches Website to Inform Public About Dangers of Transvaginal Mesh

The Rottenstein Law Group, which represents clients with claims stemming from the harmful adverse effects of surgical mesh, has launched a new website designed specifically to inform the public about the devices and the unfortunate severe consequences that can result after implantation.