Capretz & Associates

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Product Liability
individual and class
action lawsuits

Capretz & Associates is representing women who had certain recalled models of Allergan’s Natrelle breast implants and later developed anaplastic large cell lymphoma (BIA-ALCL).

Allergan, based in Dublin, Ireland, allegedly knew that its Biocell textured breast implants, in tens of thousands of women, increased the chances of their developing anaplastic large cell lymphoma (BIA-ALCL) but failed to warn the women or their doctors about those risks.

Allergan recalled its implants on July 24, 2019.

Recalled Products include:

Allergan Natrelle BIOCELL Textured Products:

  1. Allergan Natrelle Saline-Filled Textured Breast Implants
  2. Allergan Natrelle Silicone-Filled Textured Breast Implants
  3. Allergan Natrelle® 410 Highly Cohesive Anatomically Shaped Silicone- Filled Textured Breast Implants
  4. Allergan Natrelle 133 Plus Tissue Expander
  5. Allergan Natrelle 133 Tissue Expander with Suture Tabs

Other pertinent information:

  1. Lot numbers: All lots (for complete listing of all styles, see the FDA Safety Communication)
  2. Manufacturing Dates: July 25, 2014 – June 21, 2019
  3. Distribution Dates: September 14, 2014- July 24, 2019
  4. Devices Recalled in the U.S.: 246,381

If you have Allergan Biocell textured breast implants and have developed BIA-ALCL, contact us immediately for a free consultation to discuss your case.  We want to help you receive the compensation that you deserve and hold Allergan accountable for their negligent actions.

Call us toll-free at 1-800-351-8588 or Click Here to provide us with your contact information so a Capretz representative can call you.

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