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Internal Bra Breast Mesh Lawsuit [2026]: Breast Mesh Surgical Implant Injury Cases

Internal Bra Breast Mesh Implant Lawsuit Cases and Settlement Claims

Have You (or A Loved One) Suffered Injury or Complications After Breast Surgery Involving An Internal Bra Breast Mesh Implant?

Internal Bra Breast Mesh Lawsuits & Settlements

Reviewed by Jacobs Kolton, Chtd. Attorneys at Law; Updated May 2026

Internal bra breast mesh lawsuits involve claims that manufacturers of certain surgical mesh products used in breast reconstruction, breast lifts, breast augmentation, breast reduction, or revision breast surgery may have failed to adequately warn that these devices can cause serious complications, including chronic pain, infection, inflammation, mesh migration, erosion, rupture, implant failure, breast deformity, and the need for revision or removal surgery.

Our team of medical device injury lawyers and class action attorneys is investigating potential internal bra breast mesh lawsuit cases and settlement claims of women who suffered from complications or injuries after having breast surgery involving an internal bra breast mesh implant.

internal bra breast mesh lawsuit case settlement claim

If you or a loved one suffered complications or injuries after having breast surgery (reconstruction, revision breast surgery, lift, augmentation, reduction, etc.) that involved an internal bra breast mesh implant, you may be entitled to recover compensation from an internal bra breast mesh lawsuit case or settlement claim.

An internal bra is a surgical support technique used during certain breast surgeries (e.g., breast reconstruction, revision breast surgery, breast lifts, breast augmentations, breast reductions, etc.) where a surgeon places surgical mesh (i.e., “breast mesh”) made of synthetic plastic or biological tissue (such as acellular dermal matrices or ADM) inside the breast to form an internal scaffold or sling to help support tissue, hold implants in position and/or provide internal structural support to prevent the breasts from sagging (ptosis) or bottoming out.

Hundreds of thousands of women are estimated to have had surgical mesh implanted in their breast tissue during breast reconstruction or other breast surgery, even though the FDA has not cleared or approved any surgical mesh for use with breast implants or in breast reconstruction surgery and has not reviewed potential benefits and risks for these uses.

Instead, such surgical mesh has been used “off-label” by surgeons in breast surgeries. And, although surgical mesh has been approved for use in certain urogynecologic surgical procedures (e.g., pelvic floor surgeries involving transvaginal mesh and transabdominal mesh), hernia repair surgeries, and/or other general and reconstructive surgeries for soft tissue reinforcement, the FDA has warned that “There are no surgical mesh products cleared or approved by the FDA for use in breast surgery, including in augmentation or reconstruction.”

Unfortunately, internal bra breast mesh has been alleged to cause serious complications in some patients, including chronic pain, infections, abscesses, seroma (chronic fluid buildup around the mesh), inflammation, capsular contracture, mesh implant failures (erosion, migration, rupture, etc.), nerve damage, tissue death, scarring and the need for additional surgery to remove, replace or repair the breast mesh.

Injured women (and, in some cases, their family members) are now coming forward and filing internal bra breast mesh lawsuits seeking compensation and justice for the harm and suffering they may have endured after having breast surgery that involved a breast mesh implant.

team of doctors performing breast surgery on patient

Internal Bra Breast Mesh Lawsuit: Overview

Internal Bra Breast Mesh Lawsuits & Settlements

Internal bra breast mesh lawsuit and settlement cases potentially being investigated include claims of women who had breast surgery involving an internal bra breast mesh implant procedure and suffered serious internal bra breast mesh problems, injuries, side-effects or complications including, among others:

If you or a loved one suffered injury or complications due to an internal bra breast mesh product, you may be eligible to recover compensation from an internal bra breast mesh lawsuit or settlement case.

Internal Bra Breast Mesh Injury Lawsuit Cases and Settlement Claims

Who May Qualify for a Breast Mesh Lawsuit

Individuals may qualify for an internal bra breast mesh lawsuit case or settlement claim if they (or a loved one):

  • Had Breast Surgery: Had breast surgery, including breast reconstruction, revision breast surgery, breast lift, breast augmentation, or breast reduction surgery.
  • Breast Mesh Was Surgically Implanted: Surgical mesh (synthetic plastic or biological tissue) was surgically implanted inside the breast to form an internal scaffold or sling in an internal bra procedure.
  • Suffered Injury: Suffered complications or injury as a result of the breast mesh, including chronic pain, infections, abscesses, seromas, capsular contracture, mesh implant failures (erosion, migration, rupture), nerve damage, tissue death, scarring and/or the need for additional surgery to remove, replace or repair the breast mesh.

Other criteria may apply in order to be eligible. Not all individuals or cases qualify for an internal bra breast mesh lawsuit. Individuals may not qualify if (1) medical factors or unclear timing make it difficult to link the injuries to the breast mesh; (2) the claim is outside the statute of limitations period (if an individual waits too long they may be legally barred from suing); and/or (3) medical records do not support the claims. Individuals may not qualify for other reasons.

Breast Mesh Internal Bra Injury Lawsuit Complaints

Women who claim to have suffered injury or complications after having breast surgery involving an internal bra breast mesh implant are filing lawsuits seeking to recover money damages for injuries suffered, including infection, chronic pain, inflammation, mesh implant failure (migration, erosion, detachment, rupture, etc.), tissue or nerve damage, breast deformity, and revision or removal surgery, among others.

Plaintiffs in the internal bra mesh lawsuit complaints may allege, among other things, that Defendants knew or should have known of the potential dangers, risks and adverse health effects of using surgical mesh for internal bra breast surgery, but failed to warn plaintiffs or their doctors of the health risks. Plaintiff may also allege that Defendants marketed or promoted mesh products for use in breast surgery, despite not having performed adequate safety testing or receiving FDA approval.

The breast mesh lawsuit cases may assert legal claims for, among other things, negligence, strict liability design defect, strict liability manufacturing defect, strict liability failure to warn, breach of express warranty, breach of implied warranty, and loss of consortium.

Companies Sued For Internal Bra Breast Mesh Injury

Defendants named in internal bra breast mesh lawsuits may include manufacturers, sellers, processors, developers and/or distributors of surgical mesh products, such as:

  • Becton, Dickinson and Company
  • Galatea Surgical
  • C.R. Bard, Inc. (Davol Inc.)
  • Integra LifeSciences
  • Allergan (AbbVie, Inc.)
  • LifeCell Corporation
  • Ethicon (Johnson & Johnson)
  • MTF Biologics
  • Other internal bra breast mesh defendants

Product Brands Involved In Internal Bra Lawsuits

Internal bra lawsuit and settlement cases potentially being investigated include breast mesh lawsuit cases and settlement claims involving the following breast mesh brands, among others:

GalaFLEX: GalaFLEX is a biologically derived mesh scaffold (framework designed to support the growth of new, healthy tissue) made from P4HB (poly-4-hydroxybutyrate), a bioresorbable polymer. GalaFLEX is used in plastic surgery, such as breast reconstruction or mastopexy, to provide initial internal support. Over time, it is replaced by the patient’s own natural collagen. GalaFLEX is manufactured by Galatea Surgical, a subsidiary of Becton, Dickinson and Company (“BD”).

GalaFORM: Similar to GalaFLEX in material composition, GalaFORM is a mesh scaffold specifically designed with a unique 3D shape. This contoured structure allows it to better fit the anatomy of the breast, providing a “sling” effect that helps maintain the shape and position of the tissue during healing. GalaFORM is made by Galatea Surgical, a subsidiary of BD.

GalaSHAPE: GalaSHAPE is another P4HB-based bioresorbable soft-tissue mesh scaffold intended for use where surgeons want added soft-tissue support and shaping in plastic or reconstructive procedures. GalaSHAPE is made by Galatea Surgical, a subsidiary of BD.

Phasix: Phasix mesh is a fully resorbable monofilament surgical mesh made from P4HB. It is primarily used for soft-tissue repair such as hernia repair and has been described as combining the repair strength of a synthetic mesh with remodeling characteristics often associated with biologic materials. Phasix is manufactured by C.R. Bard, Inc. (Davol), a division of BD.

Phasix ST: Phasix ST is a bioresorbable mesh with a hydrogel barrier designed for intra-abdominal soft-tissue repair, including hernia repair. The mesh provides temporary support while the Sepra Technology-based barrier is intended to reduce tissue attachment on the visceral side during healing. Phasix is made by C.R. Bard, Inc. (Davol), a division of BD.

DuraSorb: DuraSorb is a 100% bioresorbable monofilament mesh engineered from polydioxanone (“PDO”), for reinforcement of soft tissue where weakness exists. It has been described as a thin synthetic scaffold intended to address limitations of permanent mesh in plastic and reconstructive applications while gradually resorbing over time. DuraSorb is manufactured by Integra LifeSciences.

AlloDerm: AlloDerm is a human acellular dermal matrix (“ADM”) used in reconstructive surgery as a tissue matrix for reinforcement and coverage of soft tissue. Alloderm ADM has been described as a regenerative tissue matrix that has been used in breast reconstruction and other soft-tissue procedures where surgeons want a biologic material rather than a permanent synthetic mesh. AlloDerm was developed by LifeCell Corporation, now owned and operated by AbbVie (Allergan).

Strattice: Unlike AlloDerm, Strattice is a reconstructive tissue matrix made from porcine dermis (pig-derived) that is processed into an acellular biologic scaffold. Strattice ADM is used in soft-tissue reconstruction, including abdominal wall and breast-related reconstructive procedures, where added support is needed. Strattice was created by LifeCell Corporation, now owned and operated by AbbVie (Allergan).

FlexHD: FlexHD is a human ADM similar to AlloDerm but processed differently. FlexHD, often described as a biologic mesh, is known for having no “sidedness” (both sides are the same), which can make it easier for surgeons to handle. It is often used for its high tensile strength and ability to integrate quickly with the patient’s blood vessels. FlexHD is processed by Musculoskeletal Transplant Foundation (MTF Biologics) and marketed and distributed by Ethicon (a Johnson & Johnson company).

AlloMax: AlloMax is another human-derived ADM used for soft tissue soft-tissue repair and reinforcement. AlloMax is processed using a gentler method intended to preserve the natural collagen structure and growth factors of the dermis, which may help facilitate faster inward growth of the patient’s cells. AlloMax is made by C.R. Bard, Inc. (Davol), a division of BD.

SurgiMend: SurgiMend is an acellular collagen matrix derived from fetal bovine dermis (skin of a cow fetus) used for soft-tissue reinforcement. Because it is derived from fetal tissue, it is naturally rich in Type III collagen, which is associated with healing and elasticity. It is frequently used in both abdominal wall reconstruction and plastic surgery. SurgiMend is manufactured by Integra LifeSciences.

Breast Surgery That May Involve Breast Mesh

Breast mesh implants have been used in a wide range of breast surgeries, including breast reconstruction, revision breast surgery, breast lift, breast augmentation, and breast reduction surgeries:

  • Breast Reconstruction (Post-Mastectomy): A breast reconstruction is a surgical procedure performed after a mastectomy or lumpectomy to rebuild the shape and look of the breast using implants or the patient’s own tissue. In post-mastectomy cases, breast mesh acts as a structural scaffold to replace lost tissue, securely holding a breast implant in place and helping to create a natural-looking curve where the breast was removed.

  • Revision Breast Surgery: A revision breast surgery is a secondary operation performed to correct, improve, or replace the results of a previous breast surgery that has experienced complications or aesthetic changes over time. This procedure uses mesh as a corrective tool to reinforce “thinned out” areas or to rebuild the internal walls of the breast pocket when an older implant has shifted, slipped, or caused tissue damage.

  • Breast Lift (Mastopexy): A breast list is a surgery to remove excess skin and tighten the surrounding tissue to raise and reshape sagging breasts for a more youthful contour. During a breast lift, the breast mesh is positioned like a hammock underneath the breast tissue to provide permanent internal suspension, preventing the skin from stretching back out and the breast from sagging again over time.
  • Breast Augmentation: A breast augmentation is a cosmetic procedure designed to increase the size, fullness, and symmetry of the breasts through the surgical insertion of implants. In certain breast augmentations, breast mesh is used to provide extra “foundation” for patients with very thin natural tissue or those receiving larger implants that require more support than the skin can provide on its own.
  • Breast Reduction: A breast reduction is a procedure that involves the removal of excess breast fat, glandular tissue, and skin to achieve a breast size more in proportion with the body and to alleviate physical discomfort. In breast reduction surgery, breast mesh is often used to reinforce the lower pole of the breast, ensuring that the remaining tissue stays elevated and maintains its new, smaller shape against the pull of gravity.

Internal Bra Breast Mesh Complications

The use of breast mesh for internal bra surgery can potentially lead to various complications and injuries, including:

  • Biological Incompatibility & Rejection of Mesh: The body does not always accept the breast mesh as a natural extension of its own tissue. In some cases, the immune system triggers a Foreign Body Response, leading to chronic inflammation as it attempts to isolate the material. If the patient’s own blood vessels and cells fail to grow into the mesh (process known as revascularization) the mesh remains a “dead” piece of material. This failure to integrate prevents the mesh from becoming a living part of the breast anatomy, eventually leading to its degradation or rejection.
  • Mechanical Failure Of Internal Bra Mesh: The physical integrity of an “internal bra” depends on the strength of the mesh and the security of its attachment points. The mesh can be compromised by several closely related mechanical failures, most notably mesh migration and displacement. Collectively, these mechanical issues can result in a total loss of breast shape, visible deformities, and often sharp, chronic pain that requires surgical intervention to retrieve or replace the failed material.
  • Mesh Migration/Displacement: Mesh migration occurs when the mesh slowly “crawls” or shifts from its original surgical position due to gravity, muscle movement, or inadequate initial fixation, whereas mesh displacement refers to a more sudden or total movement of the mesh away from its intended site. During this movement, the mesh can also experience folding or bunching, where the material crumples onto itself. These folds can create sharp edges or hard lumps that are palpable through the skin, leading to chronic irritation and mechanical discomfort for the patient.
  • Mesh Detachment: The loss of positioning of the mesh often leads to mesh detachment, where the sutures or tacks holding the material to the chest wall or breast tissue snap or pull through, causing the internal support to collapse.
  • Mesh Erosion and Rupture: In severe cases, the mechanical stress of the mesh can cause it to wear through adjacent structures, a process known as mesh erosion. This occurs when the mesh rubs against the breast implant, potentially causing an implant rupture, or when it thins the overlying skin until the mesh becomes exposed. While less frequent with modern biologics, mesh rupture can occur in synthetic materials where the scaffold physically tears or breaks under high-pressure loads, resulting in a total and sudden collapse of the internal support structure.
  • Mesh Attenuation and Over-Stretching: Mechanical failure can also result from the physical stretching of the mesh material over time, a process known as attenuation. If the mesh lacks sufficient “tensile strength” to support the weight of the breast implant, the fibers will slowly elongate under the force of gravity. As the mesh stretches, it becomes thinner and weaker, eventually losing its ability to hold the implant in the correct position. This leads to a loss of the surgical lift and a distorted breast shape as the “sling” fails to maintain its original dimensions.
  • Inflammation: Inflammation is a common complication associated with breast mesh, as the body may recognize the material as a foreign object and mount an immune response. This can lead to symptoms such as redness, swelling, warmth, and pain in the affected breast. While some inflammation is expected after breast surgery, persistent or excessive inflammation may indicate an ongoing reaction to the mesh, irritation of surrounding tissues, or even early infection. Chronic inflammation can interfere with healing, contribute to scar tissue formation, and increase the risk of additional complications, sometimes requiring medical treatment or surgical removal of the mesh.
  • Bacterial Infection and Biofilm Formation: Because internal bra mesh is often porous, it provides a vast surface area where bacteria can hide and multiply. If even a small amount of bacteria enters the surgical site, it can colonize the mesh and create a biofilm, which is a protective layer that shields the bacteria from the body’s immune system and standard antibiotics. Once a biofilm has formed on the mesh, the infection is often impossible to clear with medication alone, frequently necessitating a secondary surgery to remove the mesh entirely.
  • Chronic Seroma and Fluid Accumulation: The presence of a foreign material can interfere with the body’s ability to reabsorb natural fluids, leading to a persistent seroma (a pocket of clear fluid). Mesh can act as a physical barrier or an irritant to the surrounding tissue, causing fluid to collect between the mesh and the breast skin or implant. This fluid buildup prevents the mesh from adhering to the chest wall, creates uncomfortable pressure, and significantly increases the risk of a subsequent infection.
  • Hematoma (Blood Collection/Bleeding): A hematoma can occur as a complication of breast mesh surgery when bleeding develops around the implanted mesh, leading to a collection of blood within the breast tissue. The presence of mesh may increase the risk or severity of a hematoma by interfering with normal tissue healing or creating spaces where blood can accumulate. This can cause swelling, firmness, bruising, and significant pain, and may place added pressure on surrounding tissues and the mesh itself. If not properly treated, a hematoma can contribute to further complications such as infection, delayed healing, or even compromise of the surgical outcome, sometimes requiring drainage or additional surgery to remove the blood and address the affected mesh.
  • Fibrosis, Scarring and Capsular Contracture: While breast mesh is sometimes used to help support an implant, it can occasionally trigger an aggressive scarring response. If the body perceives the breast mesh as a significant irritant, it may produce excessive amounts of dense, fibrous scar tissue. This can lead to capsular contracture, where the area becomes hard, tight, and painful. In severe cases, the contraction of the scar tissue around the mesh can distort the shape of the breast, causing visible ripples or an unnatural, “frozen” appearance.
  • Mesh Adhesion and Inability to Remove: Mesh can become permanently fused to the body when it becomes extensively integrated with surrounding tissue through scar formation and fibrosis. While some level of tissue in-growth is expected, excessive or abnormal fusion can cause the mesh to adhere tightly to muscles, nerves, and breast tissue, making it difficult or even impossible to remove without causing further tissue damage, bleeding, or additional nerve injury. This can lead to chronic pain, restricted movement, and ongoing inflammation, as the body continues to react to the foreign material. In severe cases, attempts to remove the fused mesh may require complex surgery and carry a risk of additional injury to surrounding structures, leaving patients with long-term complications.
  • Tissue Necrosis and Poor Perfusion: The success of an internal bra procedure relies heavily on the health of the overlying skin, particularly in reconstructive cases following a mastectomy. If the mesh exerts too much pressure against the skin, or if the surgical site has poor blood flow (perfusion), the skin may begin to die, a condition known as necrosis. This can lead to the mesh becoming exposed through an open wound, which is a serious complication that almost always requires the immediate removal of the mesh and the implant to prevent further systemic injury.
  • Premature Degradation: Premature degradation occurs when the breast mesh loses its structural integrity and dissolves far sooner than intended. In procedures using certain dermal matrix or “biologic” meshes, the material is designed to act as a temporary scaffold that stays strong while your body replaces it with its own collagen. However, if the body’s enzymes break down the mesh before the natural tissue has become strong enough to take over the weight-bearing load, the “internal bra” effectively disappears. This leaves the breast without support, leading to a quick recurrence of sagging or a total failure of the surgical lift.
  • Corrective or Revision Surgery: When an internal bra mesh fails or causes significant complications, a complex secondary surgery (often termed a revision mammaplasty or mesh explantation) may be required to stabilize the breast and protect the patient’s health. Depending on the severity of the issue, the surgeon may need to carefully “debride” or scrape away failed mesh fragments that have become embedded in the chest wall or breast tissue, a process that is particularly delicate if the mesh has partially integrated or become infected. If the complication involves capsular contracture or a biofilm, the surgeon must often perform a total capsulectomy, removing the entire scar tissue envelope along with the mesh and the implant. In cases where the mesh was intended to provide structural support that has now vanished, the surgeon may have to “re-suspend” the breast using different techniques, such as a traditional mastopexy (breast lift) or by substituting the failed material with a new, more compatible graft. These procedures are often more time-consuming than the original surgery because of the presence of distorted anatomy, scar tissue, and the need to restore a blood supply to damaged skin flaps.
  • Nerve Damage: Nerve damage can occur as a serious complication of breast mesh used in internal bra procedures, particularly when the material fails, shifts, or triggers an inflammatory response. The breast mesh may irritate or compress nearby nerves in the breast and chest wall. This can lead to symptoms such as persistent pain, burning sensations, numbness, or hypersensitivity in the breast or nipple area. In some cases, scar tissue may form around the mesh, further entrapping nerves and worsening discomfort. Nerve damage can be severe and long-lasting, sometimes requiring surgery.
  • Delayed Wound Healing: Delayed wound healing is a possible complication associated with breast mesh when the presence of the material interferes with the body’s normal healing process. The mesh, as a foreign object, can trigger prolonged inflammation or reduce adequate blood flow to the surrounding tissue, making it more difficult for the surgical site to close and repair properly. This can result in wounds that take longer to heal, remain open, or are more prone to breakdown and infection. In some cases, delayed healing may lead to exposure of the mesh, increased scarring, or the need for additional medical treatment or surgical intervention to promote proper recovery.
  • Red Breast Syndrome (RBS): Red breast syndrome is a unique, non-infectious inflammatory complication specifically linked to the use of biologic mesh, such as Acellular Dermal Matrix (ADM). It typically presents as a bright, painless redness (erythema) on the skin directly overlying the area where the mesh was implanted.
  • Breast Disfigurement, Deformity or Asymmetry: Breast disfigurement, deformity or asymmetry can occur as a complication of breast mesh when the material shifts, contracts, or integrates unevenly with the surrounding tissue. Instead of providing uniform support, mesh may distort the natural shape of the breast, leading to visible irregularities such as uneven size, contour abnormalities, or displacement of breast tissue, including distorted, drooping, or lopsided breasts. Scar tissue formation around the mesh can further contribute to tightening or pulling, worsening the asymmetry over time. These changes can affect both the appearance and feel of the breast and may require corrective surgery to remove or reposition the mesh and restore a more natural, balanced contour.
  • Bottoming Out and Displacement: When the mesh fails to provide a firm lower boundary, the result is a complication called “bottoming out.” This occurs when the mesh (the internal bra) either stretches excessively or slides down the chest wall, allowing the breast implant to drop below the intended inframammary fold. This displacement shifts the entire volume of the breast toward the abdomen, often causing the nipple to look as though it is pointing upward and creating an unnatural, elongated appearance of the lower breast.
  • Breast Implant Loss (Reconstruction Failure): Breast implant loss or failure of a breast implant reconstruction in which the breast implant (the silicone or saline device used to create or restore breast volume) must be surgically removed can occur as a result of complications related to breast mesh, such as inflammation or inadequate support. When the surrounding tissue is unable to properly heal or sustain the breast implant, removal becomes necessary to prevent further damage or serious complications. Implant loss often represents a setback in the reconstruction process and may require additional surgeries, delayed reconstruction, or alternative techniques to restore the breast.
  • Chronic Breast Pain: Chronic breast pain is a potential complication associated with the use of breast mesh, as the material may cause irritation, inflammation, or abnormal scar tissue formation. Patients may experience ongoing discomfort ranging from dull aching to sharp or burning sensations in the breast or chest wall. This pain can result from the mesh placing pressure on surrounding tissues or nerves, or from the body’s reaction to a foreign material. Chronic pain related to mesh can persist for months or years and may interfere with daily activities, sleep, and overall quality of life, sometimes requiring additional treatment or surgical removal of the mesh.

FDA Warnings About Internal Bra Breast Mesh

In recent years, the FDA issued various safety communications highlighting that the safety and effectiveness of surgical mesh products (including synthetic plastic and biologic versions) in breast surgery have not been established. For instance, on March 31, 2021, the FDA issued a safety communication to inform the public and health care providers about the higher chance for complications or problems related to the use of certain acellular dermal matrix (ADM) products, a type of surgical mesh, in implant-based breast reconstruction surgery.

Similarly, on November 9, 2023, the FDA issued a letter to healthcare providers warning them that despite the ‘increased use of surgical mesh products in breast surgery” such surgical mesh products “have not been determined by the FDA to be safe and effective for use in breast surgery.”

Studies About Breast Mesh Injuries

Published studies have reported a range of complications associated with the use of the surgical mesh in “internal bra” breast surgery, including chronic fluid buildup (seroma), infection, hardening of the breast tissue (capsular contracture), implant loss, tissue death (necrosis) and need for reoperation, among others.

For instance, a 2024 Aesthetic Surgery Journal Open Forum systematic review and meta-analysis of data from dozens of clinical studies of synthetic mesh in breast reconstruction surgery found that nearly 10% of patients using synthetic mesh in reconstruction required a second surgery (reoperation) to fix issues, 4% developed an infection, 3% developed a seroma, and 3% needed a total explant where the breast implant is removed entirely. Studies have also found that certain biologic mesh brands used in implant-based breast reconstruction surgery were linked to even higher rates of major complications (which include infection, reoperation, and total implant removal).

Compensation Possible For Internal Bra Breast Mesh Injury Lawsuit Cases

Compensation For Breast Mesh Injury Claims

Plaintiffs who bring internal bra breast mesh lawsuits may be able to recover compensation for injuries suffered, including money damages for:

  • Pain and suffering
  • Loss of wages or earnings due to missed work
  • Loss of future earning capacity
  • Medical care expenses incurred or to be incurred
  • Other out of pocket expenses
  • Loss of quality or enjoyment of life
  • Disfigurement/scarring/asymmetry
  • Mental anguish/emotional distress
  • Loss of consortium
  • Other possible breast mesh monetary damages

Time Is Limited To File An Internal Bra Lawsuit

Various deadlines (called statutes of limitation and statutes of repose) may limit the amount of time that women have to file a internal bra breast mesh lawsuit to try to recover compensation for complications and injuries they claimed to have suffered from breast mesh products.

This means that if a breast mesh internal bra lawsuit claim is not filed before the applicable time limit or deadline, the injured party may be prohibited from ever pursuing litigation or taking legal action regarding their breast mesh injury claim. That is why it is important to connect with an internal bra breast mesh injury lawyer or attorney as soon as possible.

If you or a loved one suffered injury or complications from an internal bra breast mesh implant, you may be entitled to recover compensation from an internal bra breast mesh lawsuit case or settlement claim. Contact a medical device injury lawyer or breast mesh injury attorney to request a free case review.

*If you or a loved one are experiencing health issues, side effects or complications from a medical device (i.e., internal bra implant or breast mesh), we urge you to promptly consult with your doctor or physician for an evaluation.

**The listing of a company (e.g., Becton, Dickinson and Company, Galatea Surgical, C.R. Bard, Davol, Inc., Integra LifeSciences, Allergan, AbbVie, LifeCell Corporation, Ethicon, Johnson & Johnson, Musculoskeletal Transplant Foundation, etc.) or product (e.g., GalaFLEX, GalaFORM, GalaSHAPE, Phasix, Phasix ST, DuraSorb, AlloDerm, Strattice, FlexHD, AlloMax, SurgiMend, etc.) is not meant to state or imply that the company acted illegally or improperly or that the product is unsafe or defective; rather only that an investigation may be, is or was being conducted to determine whether legal rights have been violated.

***The use of any trademarks, tradenames or service marks is solely for product identification and/or informational purposes.

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Have You or a Loved One Suffered Injury or Complications After Having Breast Surgery Involving an Internal Bra Breast Mesh Implant?
You May Be Entitled To Recover Money From an Internal Bra Breast Mesh Injury Lawsuit Case or Settlement Claim!
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name of mesh manufacturer, if known:
brand name of mesh, if known:
date of surgery when internal bra breast mesh was implanted:
mesh was used for:
after surgery involving the use of breast mesh, did you suffer:
date breast mesh was or will be removed, replaced or repaired:
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