Power Morcellator Lawsuits: Dangerous Surgical Device Linked to Increased Cancer Risks

Power Morcellator used during minimally invasive surgery

What Is a Power Morcellator?

Power morcellators are medical devices that are used during laparoscopic surgeries. The device is used to break up tissue into smaller pieces, which can then be removed through the smaller incisions involved in minimally invasive surgeries. Johnson & Johnson is one of the biggest manufacturers of morcellation devices, and the devices are used in tens of thousands of procedures every year.

Power morcellators have allowed doctors to use smaller cuts during surgery, which can help patients:

  • Recover more quickly
  • Avoid some complications
  • Experience less pain after a procedure 

Types of Surgeries Using Power Morecellation

Power morcellation is used in some types of laparoscopic surgery, such as kidney and spleen surgeries, but the main concern with the device has to do with its use in:

  • Hysterectomies
  • Uterine fibroid surgery

Cancer Risks Associated With the Use of Power Morcellators in Gynecological Surgeries

Unfortunately, despite the benefits, there is also evidence that the device could spread an aggressive form of cancer in some patients who undergo gynecological surgery for uterine fibroids—and some women have already lost their lives or have already developed advanced cancer that is potentially related to the device.

According to the U.S. Food and Drug Administration (FDA), one in 350 women who go in for fibroid surgery has uterine sarcoma that is not diagnosed in preoperative testing. When a power morcellator is used in surgery for a woman with this aggressive form of cancer, there is a chance that the morcellator will break up cancerous tissue, and that tissue can then “seed” cancerous growth throughout the pelvis and abdomen.

Due to the increased risk of advanced-stage cancer and the reduction in long-term survivability for victims, the FDA has officially discouraged use of the device in certain gynecologic surgeries. At this time, there are no reliable methods for positively detecting every instance of uterine sarcoma prior to fibroid surgery or thoroughly containing potentially cancerous morcellated tissue.

As of May 27, 2015, it was reported that the Federal Bureau of Investigation (FBI) had also begun investigating whether device makers violated the law by failing to report the dangers of power morcellation. While a Johnson & Johnson spokesperson said that the company was unaware of the FBI investigation, some victims and doctors had already spoken to investigators about their experiences with power morcellators. The FBI, following its official policy for speaking about potentially active cases, has neither confirmed nor denied that an investigation is ongoing.

Johnson & Johnson Recalls Power Morcellator Devices

As a result of the FDA's warning, Johnson & Johnson suspended sales of the device, and all power morcellators produced by the company's Ethicon division have now been recalled, including the following:

  • Morecellex Sigma
  • Gynecare X-Tract
  • Gynecare Morecellex

However, some victims have alleged that Johnson & Johnson did not perform adequate testing and continued to produce the potentially dangerous device even after the cancer risks were known. These three models and other brands of power morcellators are still being used in gynecologic surgeries across the nation.

Lawsuits Being Filed by Victims of Power Morcellator Devices

Lawsuits have already been filed around the nation from both victims and the families of victims who have died from the use of this potentially dangerous device. These lawsuits allege that the manufacturer knew or should have known that these devices posed a risk to patients. Additionally, evidence of the link between morcellation and some forms of cancer has been growing, and some victims have been active in campaigns to stop all use of morcellation in fibroid surgeries. The Johnson & Johnson recall is an important step in getting medical facilities and surgeons to make changes that potentially avoid cancer risks.

Although Johnson & Johnson power morcellators have now been recalled and many hospitals are discouraging the use of morcellation, laparoscopic power morcellators have been in widespread use for many years, and it is likely that other victims will come forward with complaints.

Contact Us To Discuss Your Power Morcellator Lawsuit. You Deserve the Best Legal Help. 

If you or a loved one developed cancer after a surgery involving a power morcellator, you need to understand your rights. Contact our nationally recognized law firm for a completely free case analysis.