Hip implants, pacemakers, surgical mesh, IUDs, spinal cord stimulators — when a medical device fails inside your body, the results can be catastrophic. Manufacturers knew the risks and sold the device anyway. We hold them accountable.
A recall is powerful evidence but doesn't automatically mean you have a case. You must also show the defect caused your specific injury. We'll evaluate both — the recall history and your medical records — in a free consultation.
Yes. The manufacturer's liability is separate from your doctor's. If the device was defectively designed or manufactured, the company bears responsibility regardless of your doctor's recommendation. You may also have a separate claim against your doctor if they failed to warn you of known risks.
Medical expenses (past and future revision surgeries), lost wages, pain and suffering, loss of enjoyment of life, and in cases of egregious corporate conduct, punitive damages. Device cases often result in significant settlements because manufacturers want to avoid public trials.
Absolutely. A recall is not required. If your device failed in a way that caused injury and that failure resulted from a design defect, manufacturing defect, or failure to warn, you have a claim. We investigate the device's history, FDA filings, and adverse event reports.
Device defect cases are complex and typically take 18 months to 3+ years to resolve. However, if your manufacturer faces mass tort litigation, you may be able to join a multidistrict litigation (MDL) that can accelerate resolution. We assess the best path for your specific situation.
Free consultation. No fee unless we win. Evidence disappears fast — don't wait.