No-Cost, No-Obligation Morcellator Cancer Lawsuit Case Review

Morcellator Cancer Lawsuit Center

Morcellator Lawsuits Filed for Cancer - Attorneys Handling Morcellator Cancer Lawsuits Offer No-Cost, No-Obligation Morcellator Cancer Case Review

Morcellator Cancer Lawsuit

Information about Cancer Lawsuits from Lawyers Handling Morcellator Lawsuits Nationwide

Morcellator devices have been recalled by Johnson & Johnson’s Ethicon division due to the risk of spreading ovarian cancer. Power morcellators are used to perform hysterectomies and to remove ovarian fibroids in approximately 60,000 patients each year. Promoted as an improvement over open surgery, morcellators mince uterine tissues into small pieces that are removed via tiny incisions. In patients with preexisting uterine cancer, this process can scatter the cancer cells throughout the abdomen, transforming a manageable, localized cancer into an advanced-stage and fatal disease. The risk of morcellator cancer has been the subject of FDA warnings, FDA medical device committee hearings, and Ethicon market withdrawals, as well as warnings and bans issued by major hospitals, individual doctors, and national patient advocacy groups.

Johnson & Johnson, the primary manufacturer of morcellators used for ovarian surgery, has issued a global recall of three laparoscopic power morcellators: Gynecare Morcellex, Gynecare X-Tract, and Morcellex Sigma. The J&J morcellator recall represents yet another major product safety recall from one of the largest medical suppliers in the nation. Late in 2013, J&J announced it would pay a total of $2.5 billion to settle 8,000 hip implant recall cases resulting from product defects in its DePuy Orthapaedics line. J&J is currently facing approximately 30,000 lawsuits for defective pelvic mesh implants that cause severe harm in women. Despite these setbacks, J&J increased sales during 2013 by 6.1%, reporting annual sales of $71.3 billion.

Attorneys handling morcellator cancer lawsuits believe that persons who were diagnosed with cancer after ovarian surgery may be entitled to compensation. If you or a loved one underwent ovarian surgery such as hysterectomy or myomectomy and were later diagnosed with cancer, you may qualify. Evidence suggests that Johnson & Johnson and Ethicon officials were aware of the risks of morecellator cancer as early as 2006, yet waited to recall the device until 2014 when the company came under FDA pressure. Each lawsuit that is filed will serve to increase Johnson & Johnson’s accountability for the safety of its product. Lawyers handling morcellator recall lawsuits provide no-cost, no-obligation case reviews. To learn if your case may qualify to file a morcellator lawsuit and to have your questions answered by an experienced morcellator attorney, contact our firm today.

Morcellator Cancer

Morcellator CancerPower morcellators used in hysterectomies and myomectomies have been linked to advanced-stage ovarian cancer. These devices have been routinely used by surgeons since 1995 but patients receiving morcellator surgeries were not warned of the cancer risk until recently. The April 2014 FDA morcellator cancer warning recommended that surgeons should stop using the devices due to the likelihood of exacerbating existing and unsuspected cancer. This page provides information about the research behind the morcellator cancer risk, details of the FDA morcellator cancer warning, and information about filing a morcellator cancer lawsuit.

Morcellator Recall

Morcellator Recall

In response to an FDA Safety Communication and further findings on the risks posed by morcellator surgery, Johnson & Johnson’s Ethicon division has issued a global recall of laparoscopic power morcellators used for hysterectomy and myomectomy. The morcellator recall applies to the vast majority of these devices in use today. Women who were diagnosed with ovarian cancer following a gynecologic surgery may have legal grounds to file a morcellator recall lawsuit. This section contains comprehensive information about the morcellator recall and details about who qualifies to file a morcellator recall lawsuit.

Morcellator Cancer Lawsuit

Morcellator Cancer Lawsuits

Women who were diagnosed with ovarian cancer following a hysterectomy or myomectomy may be eligible to file a morcellator cancer lawsuit. Ovarian cancer is difficult to detect prior to surgery; the use of a device that is known to spread and advance ovarian cancer has been deemed dangerous and has been recalled globally. If you or a loved one developed ovarian cancer following ovarian surgery, you may have legal grounds to file a morcellator cancer lawsuit.

Morcellator Cancer Lawyers FAQ

Morcellator Lawsuit FAQs

The morcellator lawsuit FAQs page provides answers to questions frequently asked of attorneys handling morcellator lawsuits for cancer claims. The section explains the cancer risk and describes who may qualify to file a morcellator lawsuit. Filing a morcellator lawsuit for cancer can help increase accountability for the safety of medical devices, and provides meaningful compensation for women and the families of women who have developed advanced-stage cancer following hysterectomy or myomectomy surgery.
Morcellator Cancer Lawyer

Morcellator Cancer Lawyers

This page offers an overview of the legal services provided by our morcellator cancer lawyer team. Working on a contingency basis, morcellator attorneys never charge legal fees unless they collect for you. Morcellator cancer lawyers are providing free case reviews for persons who believe they may have a morcellator claim. When you contact the firm, an experienced morcellator cancer attorney will answer your questions as definitively as possible.