Practice Area
Dangerous Drugs & Defective Medical Devices Cases
Holding Drug and Device Manufacturers Accountable
Defective Drugs & Medical Devices
We represent patients harmed by defective drugs and medical devices through design flaws, manufacturing defects, or failure to warn about serious side effects. Our experienced team takes on pharmaceutical giants and medical device manufacturers to secure justice for those who trusted these products with their health.
Current Dangerous Drugs & Defective Medical Devices Cases
Active litigation against manufacturers of dangerous drugs and devices
Depo-Provera
Birth control injection linked to increased risk of meningioma brain tumors in women who used the contraceptive.
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Paragard IUD
Intrauterine device causing breakage, migration, and serious complications during removal requiring surgical intervention.
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PowerPort
Implanted port catheter causing fractures, migrations, and life-threatening complications including pulmonary embolisms.
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Truvada
HIV prevention medication causing kidney damage and bone density loss in patients taking the drug long-term.
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Zantac (Ranitidine)
Popular heartburn medication recalled due to NDMA contamination linked to various cancers in long-term users.
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NEC (Necrotizing Enterocolitis)
Life-threatening intestinal condition in premature infants linked to cow's milk-based baby formula products.
Learn MoreOur Pharmaceutical Litigation Approach
Thorough Investigation
We conduct comprehensive investigations into drug and device safety, working with treating physicians and researchers.
Medical Documentation
Our team helps gather and organize medical records, scientific literature, and other evidence to build strong cases.
Taking on Big Pharma
We have the resources and experience to take on major pharmaceutical companies and medical device manufacturers.
Nationwide Representation
We represent clients across all 50 states in pharmaceutical and medical device litigation.
Related Knowledge
Educational articles about dangerous drugs and medical devices
Pharmaceutical Knowledge
How drug mass torts develop, FDA processes, adverse reactions, and off-label marketing issues.
Read ArticlesMedical Device Knowledge
Device regulation, common failures, implantable devices, and revision surgery considerations.
Read ArticlesHow Pharmaceutical Mass Torts Develop
Safety signals, FDA action, MDLs, and how individual drug-injury claims are evaluated.
Read ArticleFrequently Asked Questions
Questions about drug and medical device claims
Do I need a recall to have a claim?
+No. A recall can be strong evidence that a product was unsafe, but many drug and device cases proceed based on studies, adverse-event reports, and internal documents even when a product stayed on the market.
What records matter most?
+Prescription or implant history, treating-physician notes, imaging, pathology, and a clear diagnosis date. Dates help show that the injury followed use of the product.
Are these usually individual lawsuits or class actions?
+Serious injury claims are more often individual mass-tort cases or MDL claims, not a single class action that pays everyone the same amount. Compensation usually depends on the injury and the proof.
How long do I have to act?
+Deadlines vary by state and by when you knew or should have known the product was connected to your injury. A case review can identify the rules that apply to you.
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