By: Kelda Doherty Merck (formerly Schering-Plough), manufacturers of the pill-free contraceptive NuvaRing, is now facing over 1,000 law suits concerning allegations that their contraceptive is
Once touted as a breakthrough in hip implants and widely available in New York, a recent study in the British Medical Journal (BMJ) found no
Nuvaring Users and Blood Clots Many women use various forms of contraception to prevent unwanted pregnancies. Like numerous medications and devices, some forms of birth
By Thamanna Husain Our hip implant revision injury litigation lawyers have noticed some stem and ball corrosion cases. Early focus was on the ball and
Have you been suffering from your ASR XL Acetabular or ASR Hip Resurfacing System from Johnson & Johnson? Trying to sue J&J for the use
Defendants Had Sought To Keep Sealed Some Documents That Show NuvaRing Estrogen Levels Were Apparently Concealed Or Misrepresented By Organon In a defeat for Defendants
Jennifer Vezina, a Vermont resident, has become the first women to file a suit for injuries from the use of the Mirena IUD in the
Stryker Rejuvenate and ABG II Modular Hhip Stem Litigation was recently coordinated in front of Judge Martinotti in the Supreme Court of New Jersey, Bergen
By: Indhira Benitez On Thursday, March 18th, at a hearing before a San Diego federal judicial panel on Multidistrict Litigation, Bayer’s lawyer, Marie Woodbury of
While the U.S. Food and Drug Administration (FDA) sets stringent requirements for approval of pharmaceuticals, it allows many medical devices to go to market without
Merck & Co. and subsidiary Schering-Plough are facing more lawsuits relating to yet another one of the company’s products, this time Vytorin. The manufacturers responsible
On January 17, 2013, the Food and Drug Administration issued a safety communication to health care providers, surgeons and patients who have received or are
By: George Mikhail The number of medical device products affected by recalls has increased the past eight quarters reaching over 123 million units recalled in
In the United States, an estimated 800,000 people rely on implantable defibrillators to regulate their heart rhythm. However, when this life-saving device starts malfunctioning, the
Invokana has now been associated with several amputations. As of May 2017, the FDA has sounded the alarm by adding warnings for this severe side effect.
The Ethicon Physiomesh has been linked to numerous device failures and patient health safety issues across the United States. In response, many patients have come
Medical errors are the third leading cause of death in the United States. They are not the patient’s fault in any way, yet the Federal
No two people are affected by hernia mesh injuries in the same way. We strive to listen to your injuries and how they are affecting your health,
Hernia mesh suits are multiplying as the serious injuries and complications pile uo from defective meshes. Significant jury verdicts and settlements from the recalled Bard Davol
Yes! If you are complaining of pain and discomfort with your hernia mesh, yes, it is failing. Hernia meshes are foreign objects that help reinforce the muscle
Clients constantly call us with stories of pain, infection, nerve entrapment, mesh migration, and intestinal erosion. They are unable to work and relations with loved
U.S. District Judge Landya McCafferty, who presides over all Atrium C-Qur hernia mesh lawsuits, is considering rescheduling the first bellwether trial to the beginning of
Previously scheduled to occur in May 2020 and July 2020, the first two bellwether jury trials for the U.S. Bard hernia mesh injury lawsuits were
German drugs and pesticides group Bayer said on Thursday it will pay around $1.6 billion to settle the majority of U.S. claims involving its Essure
The US District Judge who oversees the multidistrict litigation (MDL) concerning the Bard hernia mesh lawsuits thinks that the number of lawsuits against the medical device manufacturer
The most common form of contraception, Intrauterine Devices (IUD), has been proven to cause dangerous outcomes in users. Medical studies have proven that unfavorable consequences
A few years ago, a group of European experts on hernia repair collaborated on a study to determine how to provide better patient outcomes in
Like many Bard hernia meshes medical devices, the PerFix Plug hernia mesh was classified as a Class II medical device and therefore exempt from rigorous testing before
A growing number of patients treated for inguinal hernia repair and had the Bard Perfix Plug hernia mesh device implanted are experiencing a variety of medical issues
The firm has many Bard Ventralight ST hernia mesh clients with filed suits for adhesions (scarring), infections and recurring hernias which have required revision surgeries.
Intrauterine Devices (IUD) are a commonly utilized form of contraception used around the world by women. However, the most common brand, Paragard, has been linked
El DIU Paragard es uno de los DIU más populares del mercado y también es el centro de muchas demandas por parte de mujeres. Muchas
Paragard is a small IUD (intrauterine device) manufactured and marketed by Cooper Surgical. The contraceptive device is touted as 100%, safe, and efficient. It is