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FDA Unlikely to Ban Power Morcellators, but Restrictions Could Come

Green power morcellator

The doctor spearheading a fight to ban some surgical tools used in minimally invasive gynecological surgery revealed that the U.S. Food and Drug Administration probably will not ban a device he calls an “absolute medical atrocity.”

Cardiac surgeon Hooman Noorchashm leads the charge against the controversial surgical tools called power morcellators, drill-like devices with spinning blades inserted through small incisions to shred and remove tissue like fibroids or uterine tissue in hysterectomies. The doctor began his fight when his wife, Amy, suffered from upstaged uterine cancer after undergoing fibroid removal with a power morcellator.

The issue with the device is that it can shred and spray cancerous tissues in the uterus and abdomen during laparoscopic surgery, causing the undiagnosed cancer to seed and spread. So far, the FDA issued a warning letter and Johnson & Johnson recalled its power morcellators.

A number of hospitals deemed use of the device risky because of how difficult it can be to diagnose some uterine cancers before surgery. Protocol is that women undergo a cancer screening, but not all cancers are detected in the screening.

Several hospital systems have already banned or taken the products off the shelf. This is little comfort to Noorchashm, who wants nothing less than an all-out ban on these devices. But he said the outcome is unlikely.

“My impression is that inside the FDA there are two groups of individuals: individuals who are more interested in advocating for industry interests and individuals who understand that the position of the FDA should be to protect patient safety and ensure patient safety. Those two groups of people are basically struggling,” Noorchashm told FierceMedicalDevices.

Even if the option to ban the devices was presented, the regulatory agency is leaning towards putting the devices under probation – although what that means for women put at risk is unclear.

Morcellator Makers Face Lawsuits

According to the FDA research, 1 in 350 women could be at risk for deadly, up-staged, uterine sarcomas. Women already died from undiagnosed uterine cancers that grew more potent and aggressive after power morcellation, spurring litigation.

Brenda Leuzzi, 44, of Perinton, New York, died in October 2014, about two years after undergoing power morcellation. She is the second Rochester-area woman to succumb to an undiagnosed cancerous tumor that is believed to have been triggered by a morcellator.

Leuzzi and her husband, George, filed a lawsuit against J&J’s Ethicon division stating the company failed to warn her that the Morcellex morcellator could spread cancer. Doctors diagnosed her with acute uterine leiomyosarcoma, a particularly deadly cancer, shortly after her hysterectomy.

Lisa and Kurt Nielsen filed a claim against Gyrus ACMI, manufacturer of the Gyrus Power Morcellator, after doctors discovered several cancerous tumors in Lisa’s abdomen following a morcellator hysterectomy. Like Leuzzi, Nielsen’s complaint stated that Gyrus failed to warn her about the dangers of the procedure and that undiagnosed cancer could spread.

Another device maker, Karl Storz, also faces lawsuits linked to its Karl Storz Rotocut Morcellator. Storz threatened Noorchashm and ordered the doctor to stop his anti-morcellation campaign, claiming it defamed the device maker.

FDA Discussed Possible Plans of Action, Doctors Divided on Risk

The FDA discussed possible solutions to the problem, including:

  • Using enhanced informed consent requirements that would educate women of the risks before surgery.
  • Using a bag attached to the morcellator to prevent spread of possibly cancerous tissues.
  • Improved testing for uterine sarcomas.

While a ban was mentioned, it was not a popular choice. The medical community is also divided on the topic.

Doctors like Robert Graebe, chairman and program director of the Department of Obstetrics and Gynecology at New Jersey-based Monmouth Medical Center, are in favor of a strict ban. “What you do about it is, you stop,” he told The Wall Street Journal. “It’s not worth playing Russian roulette with the patient.”

But the devices have strong supporters.

Elizabeth Pritts an OG/GYN with the Wisconsin Fertility Institute, published a paper in the Journal of Minimally Invasive Gynecology, and according to her findings “there is no reliable evidence that morcellation (power or otherwise) significantly results in tumor upstaging.”

Meanwhile, the FDA is considering its options before making a decision, though it does not appear to be in any hurry and makes no promises.

“If the FDA decides to take further action, we will issue communication to inform manufacturers and the public, including notice in the Federal Register,” an FDA spokeswoman said in email to FierceMedicalDevices.

Michelle Llamas, Senior Content Writer
Written By Michelle Llamas Senior Writer

Michelle Llamas has been writing articles and producing podcasts about drugs, medical devices and the FDA for seven years. She specializes in fluoroquinolone antibiotics and products that affect women’s health such as Essure birth control, transvaginal mesh and talcum powder. Michelle collaborates with experts, including board-certified doctors, patients and advocates, to provide trusted health information to the public. Some of her qualifications include:

  • American Medical Writers Association (AMWA) Engage Committee and Membership Committee member
  • Centers for Disease Control and Prevention (CDC) Health Literacy certificates
  • Original works published or cited in The Lancet, British Journal of Clinical Pharmacology and the Journal for Palliative Medicine

3 Cited Research Articles writers follow rigorous sourcing guidelines and cite only trustworthy sources of information, including peer-reviewed journals, court records, academic organizations, highly regarded nonprofit organizations, government reports and interviews with qualified experts. Review our editorial policy to learn more about our process for producing accurate, current and balanced content.

  1. Singer, P. (2014, October 27). Perinton woman who underwent morcellation dies. Democrat and Chronicle. Retrieved from
  2. Nielsen v. Gyrus ACMI, LP, et al (2014, October 9). United States District Court Eastern District of California, case no. 2:14-cv-02375-GEB-DAD. Retrieved from
  3. Saxena, V. (2014, November 7). Power morcellation ban unlikely, but other FDA restrictions coming soon. Fierce Medical Devices. Retrieved from
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