Power Morcellator Lawsuits
Orlando Personal Injury Lawyers Handling Defective Medical Device Cases
Patients should be able to expect that when they go to the hospital for
a procedure, they will not have their safety compromised by a device used
in their surgery. Unfortunately,
defective medical device cases are all too common. Thousands of people have been injured by medical machines
and tools that were not designed properly or have an unintended consequence
that put people at risk of serious harm. One of these devices is the power
morcellator, which is produced by several companies throughout the United
States, the largest of which is Johnson & Johnson’s subsidiary,
If you or a loved one have developed cancer after a surgery where a power
morcellator was used, you have the right to pursue compensation. The Maher
Law Firm has more than 40 years of experience fighting for those who have
been harmed by
dangerous medical devices and
medical malpractice. We are prepared to do whatever it takes to pursue maximum compensation
on your behalf.
Call an Orlando personal injury attorney at the Maher Law Firm today to
see if you have a case: (855) 338-0720.
Laparoscopic Uterine Power Morcellation Devices Linked to Spread of Cancerous Tissue
When a woman suffers from painful fibroids on her uterine wall, her doctor
may recommend surgical removal. In order to avoid the invasiveness and
lengthy recovery time associated with traditional fibroid removal surgery,
many doctors have turned to less-invasive techniques involving power morcellators.
Morcellators work by dividing tissue into small fragments inside of the
body before it is removed. The problem with this method is that if any
of the shredded tissue is malignant (cancerous) and is not removed, it
could migrate to other areas of the body. This could cause cancer to spread,
significantly worsening a patient’s prognosis.
In 2014, the Food and Drug Administration (FDA) released a safety communication
concerning power morcellator devices and the many dangers they pose to
women. Because there is no reliable way for doctors to predict whether
or not a woman has uterine cancer, the FDA discourages use of the device.
As many as one in every 350 women have developed unsuspected cancer in
their pelvic and abdominal regions after a surgery where the device was used.
Uncompromising Advocacy on Behalf of the Injured
In spite of the FDA’s warning, several companies continue to manufacture
the product and they are still used by many doctors in laparoscopic hysterectomy
and myomectomy procedures.
You should not have to suffer because of a dangerous medical device that
should not be allowed on the market. To learn how the Maher Law Firm can
help you pursue justice in the form of financial compensation, please call
an Orlando personal injury attorney at our firm to schedule a
free consultation. After a thorough review of your case, we can determine if you are eligible
to pursue compensation for damages including past and future medical care,
pain and suffering, lost wages, and more.
Click here to fill out an online consultation form.