Johnson & Johnson

August 30, 2014

Boston Scientific Wins 2nd Trans Vaginal Mesh Lawsuit

According to a Massachusetts jury, Boston Scientific’s vaginal-mesh sling was not defectively designed and the company properly warned about its health risks. This verdict marks a second victory for the company in two state trials over the vaginal mesh inserts.

Jurors in state court in Woburn, Massachusetts, cleared Boston Scientific of any liability for Maria Cardenas’s injuries. Cardenas, had the Boston Scientific’s Obtryx sling implanted to fix urinary incontinence problems. According to Cardenas, the sling caused her pain and she was forced to have it removed surgically.

Transvaginal Mesh and Sling Defects

August 13, 2014

New York Xarelto Uncontrollable Bleeding Lawsuit

by Dr. Shezad Malik

A Texas woman is the latest to sue Bayer and Johnson & Johnson pharmaceutical companies, claiming that the anticoagulant Xarelto has inadequate warnings about the bleeding risk associated with the drug. Jeanne Jeffcoat filed the lawsuit in the U.S. District Court for the Eastern District of New York, she claimed that Xarelto caused life-threatening bleeding event that left her permanently injured.

There are many defective drug product liability lawsuits filed nationwide over bleeding and hemorrhage side effects of Xarelto.

Xarelto Aggressive Marketing

August 1, 2014

Xarelto Bleeding Wrongful Death Lawsuit

by Dr. Shezad Malik

A Vermont man who suffered deadly brain bleed has filed a wrongful death lawsuit. The family alleges that the death was caused by side effects of Xarelto, a new generation anticoagulant. Xarelto, has recently come under fire from its irreversible bleeding side effects and is the subject of many similar lawsuits.

Thomas C. Dunkley’s daughter Ruth McGowen, filed a claim against Bayer Healthcare and Johnson & Johnson’s Janssen Pharmaceuticals subsidiary on July 25, in the U.S. District Court for the District of Vermont.

According to the Xarelto allegations, Dunkley was prescribed the blood thinner anticoagulant in July 2012, for treatment of atrial fibrillation to reduce the risk of a embolic stroke.

June 18, 2014

Illinois Ovarian Cancer Injury Talcum Baby Powder Lawsuit

by Dr. Shezad Malik

An Illinois woman has filed a lawsuit against Johnson & Johnson over their talcum powder products. Lynne Cebulske alleges that she developed ovarian cancer after using Johnson’s Baby Powder and Shower to Shower body powder for feminine hygiene purposes.

Cebulske filed the complaint in St. Clair County Court in Illinois on May 14. Throughout the United States there are a growing number of talcum baby and body powder lawsuits filed by women who allege that Johnson & Johnson failed to warn about the ovarian cancer risk associated with the talcum products.

Cebulske was diagnosed with ovarian cancer on May 14, 2012, after using Johnson & Johnson’s talcum powder products since 1992.

June 12, 2014

Endo AMS Settles Vaginal-Mesh Injuries Lawsuits

by Dr. Shezad Malik

Endo Health Solutions Inc., said it will pay about $830 million to settle most transvaginal lawsuits. Thousands of injured women allege that its vaginal-mesh implants eroded, left them incontinent and made sex painful.

https://www.youtube.com/watch?v=0Xvv9cd07G8&feature=player_detailpage

Endo’s American Medical Systems Inc. unit reported that it’s settling about 20,000 law suit product liability injury claims over the medical devices, which include the Perigee, Apogee and Elevate implants. Endo, a medical device company based in Ireland, is still exposed to at least 5,000 injury claims against AMS, including some that have been consolidated for pretrial proceedings in West Virginia.

June 6, 2014

J&J Ethicon Trans Vaginal Mesh MDL Trial Set For August

by Dr. Shezad Malik

Johnson & Johnson and its Ethicon subsidiary are exposed to more than 17,500 Ethicon pelvic mesh lawsuits in the federal court system.

Thousands of injured women have filed Ethicon Gynecare mesh product liability lawsuits for transvaginal repair, pelvic organ prolapse (POP) and female stress urinary incontinence (SUI) damage symptoms after the mesh surgeries.

The Ethicon Gynecare pelvic mesh and bladder sling products have been under fire for causing severe and debilitating injuries when the mesh erodes through the vagina, causing serious infections and the need for revision surgeries.

May 1, 2014

J & J Ethicon Stops Hysterectomy Power Morcellators Over Cancer Risk

by Dr. Shezad Malik

Johnson & Johnson’s Ethicon subsidiary has announced that it will stop selling its power morcellators used for uterine fibroid removal surgery. Medical research has shown that use of the devices during minimally invasive laparoscopic hysterectomy and myomectomy procedures may carry a risk of spreading sarcoma cancer.

Johnson & Johnson Ethicon: No Recall

The company, which manufactured and sold uterine fibroid surgery morcellators since 1998, has stopped sales, promotion and distributing the medical devices after an April 17 FDA warning. The FDA warned doctors to avoid the devices because of the risk of spreading preexisting uterine sarcomas.

April 30, 2014

FDA: Reclassification of Trans Vaginal Mesh as High Risk Device

by Dr. Shezad Malik

The U.S. Food and Drug Administration today issued two proposed orders to address the health risks associated with surgical mesh used for transvaginal repair of pelvic organ prolapse (POP). If finalized, the orders would reclassify surgical mesh for transvaginal POP from a moderate-risk device (class II) to a high-risk device (class III) and require manufacturers to submit a premarket approval (PMA) application for the agency to evaluate safety and effectiveness.

What is Pelvic Organ Prolapse?

April 8, 2014

Topamax Settlement In Cleft Lip Birth Defect Lawsuits

by Dr. Shezad Malik

Johnson & Johnson and its subsidiary Janssen Pharmaceuticals have agreed to settle Topamax birth defect lawsuits. Plaintiffs alleged that Topamax epilepsy drug side effects birth defects including cleft lips, cleft palates and other congenital malformations.

The Topamax global settlements were announced last week in Pennsylvania state court, stating that agreements have been reached in 76 complaints. According to a report, the drug manufacturers are exposed to face at least 60 additional cases that are centralized in Philadelphia.

State Court Bellwether Trials

April 5, 2014

J&J Loses Texas Transvaginal Mesh Incontinence Sling Lawsuit

by Dr. Shezad Malik

Good news for Transvaginal mesh and sling plaintiffs and it’s more bad news for Johnson and Johnson’s (J&J) Ethicon division in its ongoing vaginal mesh debacle. The company will have to pay out again, in these many cases to go to court over its allegedly defective transvaginal mesh products and urinary incontinence slings.

https://www.youtube.com/watch?v=0Xvv9cd07G8&feature=player_detailpage

Johnson & Johnson, the world’s biggest maker of medical products, was ordered by a Texas jury to pay $1.2 million to a woman who alleged that vaginal-mesh implants to treat incontinence was defectively designed. This was the first verdict against the company over those devices.