The Breast Implant lawsuits claim textured breast implants can cause anaplastic large cell lymphoma (ALCL), a rare form of non-Hodgkin’s lymphoma.
Our law firm is representing women that received textured breast implants and have subsequently been diagnosed with ALCL. We have been handling lawsuits against medical device manufacturers since 1955. We are listed in Best Lawyers in America and The National Trial Lawyers Hall of Fame.
What Do We Know About the Breast Implant Lawsuits
According to the World Health Organization and United States Food and Drug Administration (“FDA”), breast implants are linked to anaplastic large cell lymphoma, a rare form of non-Hodgkin’s lymphoma typically located in the scar capsule surrounding the implant. The illness has been termed breast implant-associated anaplastic large cell lymphoma (“BIA-ALCL”). This illness has predominantly been reported in patients with textured breast implants, although there have been some ALCL reports involving women who have received smooth breast implants.
In 2016, the World Health Organization officially designated BIA-ALCL as a form of T-cell lymphoma that can develop following breast implantation. In December 2018, sales of textured Allergan breast implants were suspended in all 33 countries in Europe as well as Israel, Brazil, and Australia. In May 2019 Health Canada suspended Allergan’s license for its BIOCELL breast implants after an internal safety review concluded that these implants conferred an increased risk of ALCL.
Allergan, a manufacturer of textured breast implants, was forced to recall their implants after numerous reports of women suffering anaplastic large cell lymphoma.
In May 2019, the FDA held a two day Advisory Committee meeting to discuss the risks and benefits of breast implants and to make recommendations regarding appropriate actions to take in light of concerns related to BIA-ALCL. On July 24, 2019, the FDA announced that it was taking action to protect patients by requesting that Allergan voluntarily recall all of its textured breast implants and associated tissue expanders from the U.S. market.
The FDA decided to request this recall after a review of newly-submitted adverse event reports involving BIA-ALCL. The FDA noted that it found “the risk of BIA-ALCL with Allergan BIOCELL textured implants is approximately 6 times the risk of BIA-ALCL with textured implants from other manufacturers marketing in the U.S. and that “continued distribution of Allergan’s BIOCELL textured breast implants would likely cause serious, adverse health consequences and potentially death from BIA-ALCL.”
Breast Implant Cancer Injuries & Treatment
Anaplastic large cell lymphoma (ALCL) is a form of non-Hodgkin's lymphoma. The disease is caused by the mutation of a specific gene which causes T-cells to produce excess amounts of a protein known as anaplastic lymphoma kinase (ALK1).
It is not known why textured implants can cause this cancer. However, research suggests that it may be linked to the inflammation that results in the formation of the scar tissue, which in turn holds the implants in place. It is also possible that bacterial contamination at the surgical site may play a role, as well as a family history of lymphoma.
Initial symptoms of ALCL usually consist of a painless, but noticeable swelling in the lymph nodes (for example, the armpit or neck). This may be followed by a loss of appetite, generalized fatigue, fever, and night sweats. An accurate diagnosis requires the analysis of an enlarged lymph node in order to determine if lymphoma cells are present.
As of August 1, 2019, a total of 573 cases of anaplastic large cell lymphoma associated with breast implants were submitted to the FDA. Of these, 481 (84%) reports involved Allergan breast implants, 50 (9%) reports involved implants manufactured by Mentor, Sientra, and other companies, and 40 (7%) reports did not identify the implant manufacturer. These BIA-ALCL reports included 33 deaths. The implant manufacturer was identified in 13 of these cases and 12 such cases involved Allergan implants. Based on the available adverse event data, the median time from implantation to diagnosis of ALCL is 8 years.
If detected early enough, BIA-ALCL can often be successfully treated by removal of the implant and surrounding scar tissue. However, ALCL can metastasize to other parts of the body and treatment with chemotherapy and radiation may be required. Early diagnosis is of utmost importance.
Compensation in Breast Implant Cancer Lawsuits
If you or a loved one experienced anaplastic large cell lymphoma (ALCL) after having breast implants, then we will be seeking the following damages for you:
- Past and future medical and funeral expenses that result from the injuries.
- Past and future pain and suffering (physical and mental) caused by the injuries, and the treatment and recovery process.
- Past and future wage loss and loss of estate (if death occurred).
- Past and future loss of earning capacity.
- Past and future loss of enjoyment of life.
- Punitive damages, if appropriate.
Breast Implant Cancer News
Allergan Recalls Textured Breast Implants Linked To Rare Type Of Cancer:
The FDA said in a statement that while the overall incidence of the cancer appears to be low, it asked Allergan to initiate the Biocell implant recall "once the evidence indicated that a specific manufacturer's product appeared to be directly linked to significant patient harm, including death." Reported in NPR
Is there any connection between breast implants and cancer? And if so, how serious is the risk?:
Research suggests that BIA-ALCL is usually found near the breast implant within the surrounding scar tissue, not the breast itself. The lifetime risk of developing BIA-ALCL from a textured implant is estimated to be from one in 1,000 to one in 30,000. Treatment involves surgical removal of the implants and the cancer. When caught early, BIA-ALCL is usually curable. Reported in Mayo Clinic
FDA and Scientific Studies Regarding Textured Breast Implants
FDA requests Allergan voluntarily recall certain breast implants
The FDA took action to protect women from breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) by requesting that Allergan, the manufacturer of a specific type of textured implant, recall specific models of its textured breast implants from the U.S. market due to the risk of BIA-ALCL. To read more, click Food and Drug Administration Alerts
Medical Device Reports of Breast Implant-Associated Anaplastic Large Cell Lymphoma
As of July 6, 2019, the Food and Drug Administration (FDA) has received a total of 573 US and global medical device reports (MDRs) of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL). This total includes all MDRs the FDA received with any mention of "ALCL" or other spelling variations (for example, "anaplastic lymphoma," or "anaplastic") in the event narrative. To read more, click Food and Drug Administration Product Information