Tennessee Allergan Breast Implant Recall Lawyer
In September 2019, Allergan issued a recall of its Natrelle BIOCELL Textured Breast Implants. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injury or death.
The FDA requested that Allergan recall all BIOCELL textured breast implants and tissue expanders marketed in the U.S. due to risk of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) a type of non-Hodgkin’s lymphoma (a cancer of the immune system). The breast implants and tissue expanders are used not only for breast augmentation, but also for reconstructive surgery after a mastectomy due to breast cancer.
If you or a loved one has had a breast implant and has been diagnosed with breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), please contact our intake specialists by phone (865) 457-6440 or by contact form.
