Allergan Textured Breast Implants Linked to Cancer

What You Need to Know

• In July 2019, the U.S. Food and Drug Administration (FDA) took action to protect patients in the United States who have had specific types of textured breast implants and tissue expanders made by Allergan.
• Evidence indicates certain Allergan textured breast implant products are directly linked to causing breast implant-associated anaplastic large cell lymphoma (BIA-ALCL).
• Allergan is issuing a worldwide product recall of its BIOCELL textured breast implants.
• If you have Allergan textured breast implants and have been diagnosed with BIA-ALCL, you may be entitled to significant financial compensation.

What Allergan Textured Breast Implants are Involved?

• The Allergan textured breast implant products include:
  • Natrelle Saline-Filled breast implants
  • Natrelle Silicone-Filled breast implants
  • Natrelle Inspira Silicone-Filled breast implants
  • Natrelle 410 Highly Cohesive Anatomically Shaped Silicone-Filled breast implants
• The Allergan tissue expanders products used by patients prior to breast augmentation or reconstruction include:
  • Natrelle 133 Plus Tissue Expander
  • Natrelle 133 Tissue Expander with Suture Tabs

What Effects have Patients Seen?

FDA evidence indicates that as of July 2019, 481 unique cases of BIA-ALCL have been attributed to Allergan implants, including a dozen patient deaths where the manufacturer of the implant is known.  Symptoms of BIA-ALCL include swelling and pain in the breasts.

What are Your Rights?

If you or a loved one has Allergan breast implants linked to cancer or have been diagnosed with breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), you may be entitled to significant financial compensation.

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