Internal Bra Mesh Failure Stories Highlight Risk of Pain, Infections and Other Problems

Growing number of women are reporting problems with GalaFLEX and other internal bra mesh products, often resulting in painful side effects that require surgical removal.

Women across the United States are coming forward to describe painful and life-altering complications after undergoing breast surgeries involving surgical mesh implants, outlining problems that are now expected to form the basis for internal bra mesh lawsuits being pursued against manufacturers of the products.

Although they were originally developed for hernia repair and soft-tissue reinforcement, internal bra breast mesh materials like GalaFLEX, Phasix, Strattice and AlloDerm have been widely marketed to plastic surgeons in recent years as “internal support scaffolds,” which could help maintain breast shape and stability following breast reconstruction, breast lifts or breast augmentation procedures.

However, the U.S. Food and Drug Administration (FDA) has not approved the surgical mesh products for breast reconstruction or augmentation procedures, and serious questions have been raised about why the products were so widely used in breast tissue without the manufacturers ever establishing that they are safe.

Internal Bra Mesh Stories

As information about the potential for lawsuits has begun to emerge, a growing number of women are now sharing stories on AboutLawsuits.com and across social platforms like Reddit and RealSelf, highlighting their experiences with internal bra failures and side effects. These woman often describe how they were never warned that breast mesh could degrade, migrate, or trigger severe inflammatory reactions, typically resulting in the need for corrective surgeries, permanent scarring and chronic pain.

In several cases, patients described being hospitalized for infections that only resolved after the mesh was surgically removed. Others say they were unaware that mesh was even used in their procedures until complications began.

In this featured post, the editors at AboutLawsuits.com have compiled several examples of the reports submitted by women who received breast mesh, which highlight the risk of pain, infections and other problems that have been linked to internal bra products.

GalaFLEX Internal Bra Stories on AboutLawsuits

These firsthand stories illustrate the physical pain and emotional trauma that many women say they never anticipated when agreeing to breast enhancement or reconstruction using internal bra mesh. In each case, recovery required multiple revision surgeries and often left permanent damage.

“I am 27 years old and had a breast lift with GalaFLEX mesh. I immediately developed infections and needed five operations, including the removal of my implants. I still have pain every day and have lost both nipples. I can’t sleep, train, or work. My life is over — eight surgeries in one year, all because of the GalaFLEX mesh. If I had known this would happen, I never would have gotten it. My whole life is destroyed. No breasts anymore, and I’m only 27.”
–Marissa (April 26, 2024) – AboutLawsuits Commenter

“Worst experience of my life from GalaFLEX mesh infection after breast lift surgery. I almost died and almost lost my breasts. Only healed after the mesh was completely taken out after five surgeries and weeks of hospitalization.”
Lind (April 3, 2024) – AboutLawsuits Commenter

“GalaFLEX mesh for breast reconstructive surgery has completely ruined my health and mental health.”
Laura (March 31, 2024) – AboutLawsuits Commenter

GalaFLEX Internal Bra Mesh Problem Described on Reddit

In one Reddit discussion about GalaFLEX mesh complications, multiple women described hard lumps, tightness, and visible cords forming beneath the skin after internal bra procedures. One user explained that she developed “long hard cords running under my skin between my skin and implant,” while others said the mesh folded or bunched inside their breast tissue.

Another commenter warned that her surgeon had advised against mesh use but she underwent the procedure anyway, later developing a hard nodule and persistent scar tissue that left one breast visibly different from the other.

“I had a surgeon I didn’t go with warn against it. I wish I didn’t get it. It left a hard nodule and stuck out. My surgeon removed from the right breast when I developed capsular contracture in the left.

1.5 years later after the revision, I have to deal with my entire bottom left breast, where the mesh is placed, hardness – probably excess scar tissue from the mesh. It would be soft otherwise This is not pleasant when my husband and I feel a difference.”
vegkittie (May 2025) – Reddit

Others said their surgeons downplayed the potential for these reactions, despite the pain and firmness that developed after healing.

Reddit Users Warn of Internal Bra Mesh Tearing and Muscle Pain

In a separate Reddit post, a woman described experiencing searing pain after her internal bra mesh appeared to rip away from her chest muscle years after implantation. She wrote that the pain was “10 out of 10 just getting into bed and lying down” after the mesh tore, and said her surgeon offered little guidance beyond acknowledging that the area was inflamed.

“The surgery for the internal bra was in October 2019 and was performed by the same dr who did a surgery the year before. The issue now is the mesh seems to have ripped away from the muscle and it hurts really bad when I cough or sneeze or move a whole lot.
–Accomplished_Yak_164 (October 2021) – Reddit

Other Reddit users urged her to find another surgeon immediately, expressing alarm that the device might have detached inside her body. Several commenters drew parallels to transvaginal mesh injuries, warning that breast mesh could be repeating the same cycle of off-label promotion and unreported complications.

FDA Warnings Substantiate Breast Mesh Injury Claims

Since late 2023, the U.S. Food and Drug Administration has warned against the use of surgical mesh products for breast augmentation, including lift, or reconstruction procedures. The agency emphasized that the “safety and effectiveness of surgical mesh in breast surgery has not been determined by the FDA,” cautioning that these materials were only authorized for soft-tissue reinforcement in other parts of the body.

This warning came after years of patient reports describing infections, tissue necrosis, and implant loss following off-label use of internal bra mesh implants. The stories shared on AboutLawsuits, Reddit, and patient forums mirror the FDA’s concerns, with women consistently reporting mesh detachment, chronic inflammation and hardened scar tissue that required multiple revision surgeries.

As the scope of reported injuries widens, breast mesh lawyers are now pursuing claims against the mesh manufacturers on behalf of women who suffered complications after surgery. The lawsuits allege that manufacturers promoted these devices for unapproved cosmetic and reconstructive uses, misrepresented them as safe and absorbable, and failed to warn about the known risks of mesh degradation in soft breast tissue.

Women may qualify for a claim if they underwent breast augmentation, lift, or reconstruction using mesh and later experienced:

• Infection or abscess formation
• Chronic pain or nerve damage
• Mesh migration or detachment
• Seroma or fluid buildup
• Tissue necrosis or reconstruction failure
• Scarring, deformity or loss of the breast implant
• Surgical revision or mesh removal surgery

Financial compensation may be available for medical expenses, corrective surgeries, lost wages, pain and suffering, and emotional distress caused by failed mesh devices.

Individuals who experienced internal bra mesh complications can request a free, no-obligation case review to determine eligibility for a lawsuit or settlement. All claims are handled on a contingency fee basis, meaning there are no fees or expenses unless a recovery is obtained.