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Surgical mesh is used to reinforce weakened tissue during hernia repair and, in some cases, breast reconstruction. It can lower the chance of a hernia coming back or help support an implant, but when the mesh itself is defective or poorly suited, patients can face pain, infection, and repeat surgery. We investigate whether a specific mesh product or a manufacturer's failure to warn contributed to your injury.
Case EvaluationHernia mesh is generally effective, but the FDA tracks a consistent set of problems reported after implantation. Recognizing these can help you connect ongoing symptoms back to the mesh itself.
Surgical mesh used in breast reconstruction has not been cleared or approved by the FDA for that specific use, even though it is commonly used to support implants during reconstruction. The FDA reaffirmed this in a 2023 communication and specifically said it was not recommending removal in patients who have no symptoms. Reported complications with breast mesh and tissue scaffolds include the following.
Regulators and manufacturers have taken action on several mesh products in recent years. These are among the more notable examples.
Symptoms can range from mild discomfort to signs that require urgent attention.
A mesh complication can affect a patient's finances well beyond the initial surgery, and compensation may address several categories of loss.
A wrongful death claim may also be available if a mesh-related complication contributed to a loved one's death.
Every mesh case starts with the product itself, and Attorney Sean M. Cleary works to identify the manufacturer, brand, and lot number involved, compare it against known recalls and safety communications, and bring in surgeons who can speak to what caused the complication.
There is no cost to you unless we recover compensation on your behalf. Contact our office to discuss your surgical mesh complication and find out what your case may involve.