Published by If you received a breast reconstruction, augmentation, or revision surgery using Strattice mesh and experienced complications—such as implant failure, chronic pain, or revision surgery—you may qualify for a Strattice lawsuit.
Our experienced product liability team is reviewing Strattice claims now. Reach out for a free, no-obligation case evaluation.
Table Of Contents
What’s the Problem?
Strattice Reconstructive Tissue Matrix—manufactured by LifeCell (now part of Allergan)—was originally cleared for hernia repair and soft-tissue reinforcement, not for breast augmentation or reconstruction. [1]
In recent years, Strattice and other surgical mesh products have been used off-label as an “internal bra” in breast surgery, despite lacking FDA approval or long-term safety data in this context. [2]
Emerging clinical research shows that mesh in the breast environment—where movement, hormonal changes and implants alter anatomy—can lead to higher complication rates, forming the basis of a potential Strattice lawsuit.
Latest Strattice Litigation Updates
- October 9, 2025 – Legal commentary noted that breast mesh products including Strattice are under investigation for mass tort litigation after studies documented higher complication rates in breast reconstructions. [2]
- June 6, 2024 – New Jersey state court designated suits involving Strattice hernia mesh as Multicounty Litigation (MCL ATL-L-3857-21), setting precedent for centralized defect litigation. [3]
- February 2024 – Complaints surfaced alleging Strattice mesh used in breast reconstruction caused premature degradation, implant malposition and surgical revisions despite assuring long-term support. [4]
Product & Usage Overview
Strattice is a biologic mesh derived from porcine (pig) dermal tissue, processed to act as a scaffold for tissue ingrowth. [1]
While cleared via the FDA’s 510(k) process for hernia repair, it has never received clearance for breast reconstruction or cosmetic breast surgery. In breast procedures, surgeons used it off-label to support implants or provide lift—often describing it as a “hammock” or “internal bra.”
Because breast tissue and implant dynamics differ greatly from abdominal wall repair, the strain, hormonal influence and constant motion can make meshes like Strattice more vulnerable to failure—leading to complications such as migration, sagging or exposure.
Injuries & Side Effects
Patients implanted with Strattice mesh in breast surgeries have reported serious complications:
– Infection or abscess formation requiring mesh/implant removal
– Seroma or persistent fluid collection around the implant pocket
– Implant malposition, sagging, asymmetry or “bottoming out”
– Mesh bunching, detachment or early resolution before tissue support complete
– Skin erosion, tissue necrosis or visible implant deformation
– Implant rupture or reconstructive failure necessitating revision or explantation
These issues often lead to additional surgeries, extended recovery, and serious emotional and cosmetic harm.
Do You Qualify for a Strattice Lawsuit?
You may qualify if you:
– Received breast reconstruction, augmentation or revision surgery where Strattice mesh was used
– Experienced complications such as infection, revision surgery, implant failure, sagging or deformity
– Have medical records identifying Strattice or similar biologic mesh use
– Are within the statute of limitations in your state to file a claim
Evidence Required for a Claim
Important documentation includes:
– Operative notes showing “Strattice,” “porcine dermis mesh,” or “internal bra” sling
– Explant or revision surgery records and pathology reports
– Imaging or photographs showing implant shift, mesh exposure or sagging
– Medical bills, treatment records and therapy notes
– Surgeon communications referencing mesh use or describing product as supportive scaffold
Damages You Can Recover
Possible recoveries in a Strattice lawsuit may include:
– The cost of revision, explantation and reconstructive surgeries
– Lost wages, reduced earning capacity or career impact
– Pain, suffering, disfigurement and diminished quality of life
– Emotional distress, loss of consortium or familial impact
– Punitive damages if misconduct or reckless marketing is proven
Legal Grounds & Liability Theories
Various legal theories may apply, including:
– Defective design: Strattice was not engineered for the unique stresses found in breast tissue
– Failure to warn: Manufacturers did not disclose off-label use was untested, or risks of migration, extrusion and implant failure
– Negligent marketing: Mesh was marketed to plastic surgeons for breast use despite lack of approval
– Strict liability: Device caused injury despite being used as intended or foreseeable
Because Strattice was marketed or used for applications never approved, the foundation for a Strattice lawsuit is strong.
Statute of Limitations & Timing
Statutes vary by state, often between one to three years after discovery of injury or surgery revision. Mesh issues may take years to fully surface, so timely consultation is vital to preserve your rights in any Strattice lawsuit.
Frequently Asked Questions
- Was Strattice approved for breast surgery? – No. Only cleared for hernia/soft-tissue repair; no mesh has FDA approval for breast reconstruction. [5]
- Do I need revision surgery to claim? – Not necessarily. If you experienced mesh-related complications or implant failure you may still qualify for a Strattice lawsuit.
- Are there class actions? – Yes, mesh litigation efforts are growing and may lead to a mass tort. [1]
- Is this mesh being recalled? – Not yet for breast applications, but investigations and regulatory scrutiny are active.
Why Act Now
If you received Strattice mesh and later suffered implant failure, revision surgery or permanent complications, now is the time to explore your legal options. Acting early strengthens your position, helps preserve vital medical records and enhances your ability to join or initiate a Strattice lawsuit.
Product liability claims against mesh manufacturers can recover compensation for medical costs, emotional distress and future care—holding companies accountable for deploying unapproved implants without full safety testing. Don’t wait—if you believe your injuries may stem from Strattice mesh use, contact a qualified attorney today.
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References
- https://www.kugelherniameshclassaction.com/allergan-strattice-biological/
- https://www.aboutlawsuits.com/breast-mesh-lawsuits-may-follow-studies-linking-internal-bra-implants-to-complications/
- https://www.njcourts.gov/sites/default/files/mcl/orders-decisions/strattice-hernia-mesh/case-management/motionto-3857-compel.pdf
- https://www.pmc.ncbi.nlm.nih.gov/articles/PMC9773854/
- https://www.medtechdive.com/news/fda-bd-surgical-mesh-breast-surgery/699538/