Shelby County Defective Breast Mesh and Implant Injury Attorneys — Attorney911 (The Manginello Law Firm, PLLC) of Houston, Texas, Brings Ralph Manginello’s 27+ Years of Federal Trial Experience and Lupe Peña’s Former Insurance Defense Background to Shelby County’s Mid-South Medical Hub: We Litigate Allergan BIOCELL Textured Implants (Recalled July 2019, MDL 2921 Before Judge Brian R. Martinotti, Bellwether October 19, 2026), AlloDerm and Strattice ADM, GalaFLEX P4HB Bioabsorbable Scaffolds, Mentor MemoryGel and Sientra OPUS, Handling BIA-ALCL (CD30+/ALK-, T-Cell Receptor Monoclonality), BIA-SCC and Red Breast Syndrome Under 21 CFR Parts 803, 807 and 814, We apply the Tennessee Product Liability Act One-Year Statute of Limitations with the Discovery Rule to Delayed-Onset Lymphoma Claims, $50M+ Total Recovered for Families and Practice Experience in the Active $10M Bermudez v. Pi Kappa Phi institutional-Liability Lawsuit — Free 24/7 Consultation, No Fee Unless We Recover Compensation for You, Hablamos Español, 1-888-ATTY-911
Defective Breast Mesh, Acellular Dermal Matrix, and Bioabsorbable Scaffold Injury Attorneys in Shelby County: The Definitive Guide for Women and Families For a woman in Shelby County navigating the aftermath of a breast reconstruction or revision surgery that has gone wrong, the silence from the medical device industry can be deafening. You may have undergone a mastectomy at a regional center in Tyler or Longview, or perhaps traveled "across the line" to Shreveport for what you were told was a routine reconstruction using the latest in "internal bra" technology. Instead, you are now facing chronic pain, persistent redness, fluid collection, or the terrifying discovery that the products implanted in your body—acellular dermal matrix (ADM) or bioabsorbable scaffolds like GalaFLEX—were never actually cleared by the FDA for use in breast tissue. At Attorney911, led by Ralph Manginello and Lupe Peña, we represent women in Shelby County who have been used as unwitting subjects in a massive, off-label clinical experiment. With twenty-seven years of continuous practice and a deep substantive command of the FDA’s 510(k) clearance pathway and the pathology of device-related injuries, our firm provides the technical and compassionate advocacy required to take on multi-billion dollar manufacturers like Becton Dickinson, Allergan,…