Power Morcellator

Parilman & Associates – Power Morcellator Lawyers

Women across the United States may be facing the possibility of having to file a power morcellator lawsuit against certain manufacturers of these surgical products.  Hysterectomy morcellator cancer concerns have arisen to the point where the United States Food and Drug Administration, or FDA, has issued a public warning regarding these heightened risks.  Any women who have had this surgical tool used in procedures such as hysterectomies or fibroid removal procedures should seek immediate medical attention.  If necessary, they should also seek the advice of experienced power morcellator lawyers if filing a power morcellator lawsuit becomes a possibility due to harm that was done.

Power morcellators are products that aid in common types of surgery performed on women.  These products help to minimize the invasiveness of procedures that remove fibroids from the uterus, and Ethicon, which is owned by Johnson & Johnson, manufactures three very popular power morcellator products, including:

  • Gynecare Morcellex Tissue Morcellator
  • Morcellex Sigma Tissue Morcellator System
  • Gynecare X-Tract Tissue Morcellator

Perhaps because of the concern regarding hysterectomy morcellator cancer issues and/or because of steps taken by power morcellator lawyers in furtherance of filing potential power morcellator lawsuits, the distribution and sale of each of these three products has been halted worldwide.

The FDA – Hysterectomy Morcellator Cancer Concerns
On April 17, 2014, the FDA issued what is known as a safety alert designed to that discouraged the use of power morcellators in procedures such as hysterectomies and myomectomies.  The reason for this hysterectomy morcellator cancer concern was data that indicated that using these products raised the risk of spreading undetected uterine sarcomas beyond the uterus.  Uterine sarcomas are commonly known as cancer cells, and power morcellator lawyers around the country have heard stories from women regarding this serious problem, prompting the filing of power morcellator lawsuits.

The data underlying this hysterectomy morcellator cancer concern reveals that approximately 1 out of every 350 women who have undergone a hysterectomy or a myomectomy for fibroids was found to have an unsuspected uterine sarcoma, or cancerous mass present.  In addition, these cancerous cells were found to exist beyond the uterus and in places such as the abdomen and pelvis.  The presence of these dangerous cells in these locations can substantially reduce any patient’s chance for long-term survival.

Power Morcellator Lawsuits and Your Legal Rights
The FDA plans to convene an advisory panel this summer in order to further investigate the potential link between the use of power morcellators and the development of cancer.  Anyone who has had this device used during surgery should not wait to learn of the results.  Instead, they should seek immediate medical attention in order to keep a close eye on anything that could be happening inside of their bodies.

For those women who may have been harmed by these products, it should be noted that taking on an enormous corporation is a tall order for an individual consumer.  If you have been harmed in this manner, contact the power morcellator lawyers at Parilman & Associates to schedule a free initial consultation.  You can either email the firm or call 800-800-DRUG.