Case Statistics

Defendant Name: Allergan
Case Number: 4:19-cv-00361
Court: U.S. District Court for the Southern District of Iowa, Central Division
Practice Area: Dangerous Drugs & Defective Products
Status: Active
Date Filed: 10/04/2019

Case Overview

On February 25, 2020, Beth Fegan was named co-lead counsel for plaintiffs in a multi-district litigation (MDL) filed against Allergan, the manufacturers of BIOCELL textured and “gummy” breast implants. The MDL is currently pending in the United States District Court for the District of New Jersey and includes both personal injury and class action plaintiffs. Plaintiffs filed a nationwide, consolidated class action complaint in May 2020.

Plaintiffs allege that Allergan’s BIOCELL implants, recalled by the FDA on July 24, 2019, cause breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), a serious cancer, and that every implant recipient is at risk of developing the disease.  Despite the FDA’s recall, Allergan refuses to reimburse patients for the true cost of implant removal or to provide them with medical monitoring or diagnostic medical care. Plaintiffs also claim that for years, Allergan possessed information and evidence demonstrating that its recalled BIOCELL implants posed a significant risk of (and caused) BIA-ALCL, but concealed that information from patients.

Following an emergency motion filed by FeganScott, on July 14, 2020 the Court found that Allergan’s communications with BIOCELL implant patients were incomplete and misleading, and ordered Allergan to correct them. In doing so, the Court reiterated the patients’ need for the information and time necessary to make educated, meaningful choices about their legal rights.

The class action suit seeks to represent all U.S. consumers who, for personal use, implanted Allergan’s BIOCELL products that have been recalled by the FDA and who have not been diagnosed with breast implant-associated anaplastic large cell lymphoma.