The FDA is preparing to release a survey into how seriously women weigh the risks of breast implant-associated cancer when deciding whether to undergo breast enhancement or replacement procedures.
A Strattice hernia mesh lawsuit claims LifeCell and Allergan knew for years about hundreds of reports of problems, and even deaths, linked to the biological mesh, but failed to warn…
A Strattice mesh lawsuit claims its pig skin biologic design led to an infection which caused injuries and the need for revision surgery to remove the mesh.
A Strattice mesh lawsuit claims the defective design and a failure by manufacturers to warn the medical community about hundreds of previously reported problems led to the plaintiff suffering permanent…
Women continue to file breast implant ALCL lawsuits two years after Allergan's Biocell implants were recalled due to the appearance of newly-diagnosed cases.
Johnson & Johnson, Teva and other drug manufacturers won a bench decision in an opioid crisis trial in California, after the judge ruled there was no evidence linking the companies'…
The FDA has announced new safety requirements for breast implants, including a patient checklist, a black box warning, and screening requirements for silicone gel ruptures.
Allergan faces an increasing number of breast implant lawsuits over the link between its Biocell textured breast implants and a rare form of lymphoma.
In a trial underway in California, several major counties are suing drug manufacturers for $50 billion, accusing them of contributing to the opioid drug crisis.
A Strattice product liability lawsuit indicates problems with the hernia mesh led to infections and hernia mesh complications which may have contributed to the death of an Arizona man.