Defective Drugs & Medical Devices
Defective drug and medical device lawsuits offer a path to compensation for patients injured by product design flaws, manufacturing defects or inadequate safety warnings. Backed by 25 years of legal experience from its founding partner, The Wilson Firm helps families navigate these complex cases.
Watch: What sets The Wilson Firm apart from other law firms
When pharmaceutical companies and medical device manufacturers fail to prioritize safety, the consequences can be life-changing for patients and their families.
Drug and medical device lawsuits help people pursue compensation for harm caused by defective designs, manufacturing problems or inadequate safety warnings. These cases often involve complex medical and scientific issues, which can make the legal process feel overwhelming without the right support.
The Wilson Firm combines 25 years of legal experience with personalized support to help clients and families pursue claims against negligent companies and manufacturers.
What Is a Defective Drug or Medical Device Case?
Defective drug and medical device lawsuits seek compensation for victims injured by dangerous products. Patients may suffer serious complications, require additional surgeries, face long-term medical treatment or experience permanent damage.
Unlike medical malpractice claims, these cases don’t allege fault on the part of the doctor or hospital that prescribed or implanted the defective drug or device. Even when a healthcare provider acted appropriately, a patient may still suffer harm because the product itself was unsafe.
Defective drug and device cases generally fall into three categories.
- Design defects: The product was inherently unsafe as designed.
- Manufacturing defects: Mistakes occurred during production or assembly.
- Failure to warn: The manufacturer failed to provide adequate safety warnings or instructions.
The Wilson Firm helps clients navigate a wide range of defective drug and medical device cases involving serious injuries, painful complications and product failures.
Defective Drug and Medical Device Cases We Handle
Our attorneys and partners have helped clients in cases involving a range of defective drugs and medical devices.
Defective Medical Devices
Bard PowerPort and Implanted Chemo Ports
More than 3,500 Bard PowerPort lawsuits have been consolidated for multidistrict litigation (MDL) in Arizona. The first trial in this MDL concluded in May 2026, with a verdict in favor of the defense.
The cases focus on design and manufacturing risks, including catheter fracture, device migration and infection, as well as allegations of inadequate PowerPort device safety information.
Hernia Mesh
Hernia mesh lawsuits allege that defective mesh products have caused serious complications, including chronic pain, mesh migration, bowel perforation, infections and the need for repeat surgeries.
One prominent hernia mesh manufacturer, BD, reached an agreement to fully settle its hernia litigation in October 2024, though new lawsuits continue to be filed despite the global settlement.
Hip and Knee Implants
Some hip and knee replacement devices have failed prematurely or caused complications involving metal debris, inflammation and revision surgery.
In 2024, orthopedic device manufacturer Exactech filed for bankruptcy amid growing lawsuits alleging that defective implants caused avoidable injuries and complications. Even so, affected patients may still have options to pursue financial recovery.
Transvaginal and Pelvic Mesh
Lawsuits involving transvaginal mesh devices allege that the products caused serious complications, including:
- Infection
- Erosion
- Chronic pelvic pain
- Organ damage
These complications have led to additional procedures. Notably, in one study published in the Central European Journal of Urology, 22.5% of 677 patients who received a pelvic mesh implant experienced complications within one to three months after device insertion.
Defective & Dangerous Drugs
Ozempic and Other GLP-1 Medications
Lawsuits involving Ozempic and related GLP-1 medications allege severe gastrointestinal complications, including gastroparesis and intestinal obstruction.
Emerging lawsuits also claim the drugs caused NAION, an eye condition known as “eye stroke” that can lead to permanent vision loss.
Depo-Provera
Long-term use of Depo-Provera has been linked to an increased risk of meningioma, a type of brain tumor. The U.S. Food & Drug Administration (FDA) approved a label change for the drug in December 2025, highlighting this risk.
Thousands of women who allege they developed brain tumors following Depo-Provera use have pursued legal action, with more than 5,500 cases consolidated in a federal MDL in 2026.
Dupixent
Dupixent lawsuits allege that the injectable biologic medication increases the risk of T-cell lymphoma and that Regeneron and Sanofi failed to adequately warn patients of the risk.
In June 2026, the U.S. Judicial Panel on Multidistrict Litigation (JPML) consolidated federal Dupixent lawsuits into an MDL.
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How The Wilson Firm Handles Defective Drug and Device Cases
The Wilson Firm stands beside people and families harmed by dangerous drugs and defective medical devices. We understand how overwhelming these cases can feel, especially when you’re already dealing with serious health complications, mounting medical bills and uncertainty about what comes next.
Our partners work closely with clients to build strong, evidence-based claims while providing clear guidance and support throughout the process. From the initial investigation through litigation, our team helps handle every stage of your case, including:
- Gathering medical records
- Reviewing product safety information
- Consulting with medical and technical experts
- Determining whether your claim may be part of a multidistrict litigation (MDL) or an individual state court action
We handle defective drug and device cases on a contingency fee basis, meaning there are no upfront legal fees and no attorney fees unless we recover compensation for you.
As a plaintiff-only firm, we never represent manufacturers or pharmaceutical companies. We are dedicated to holding companies accountable by securing fair compensation for patients and families impacted by negligence.
When drug companies sell poorly designed, inadequately tested or improperly labeled products, it’s the consumer who pays the price. The Wilson Firm brings 25 years of experience in defective drug and medical device litigation, seeking meaningful compensation and giving a voice to injured victims and their families.
Anywhere in the nation where we have cases going on, I will be there to make sure that the rights of our clients are represented and pushed forward.
Brian Ranger Wilson, Esq., Founder of The Wilson Firm
Signs You May Have a Case
You may have grounds for a prescription drug lawsuit or device claim if any of the following apply to your situation:
- You used a drug or had a device implanted and suffered serious side effects, complications or injuries.
- The FDA issued a recall or safety warning for your drug or device.
- Your device failed, fractured, migrated or required early removal.
- You were not warned of known risks before using the drug or getting the device implanted.
- Your injuries required additional surgery, hospitalization or ongoing medical treatment.
Defective drug and device claims are subject to legal deadlines, known as statutes of limitations, which vary by state and case type. Waiting too long can affect your ability to pursue compensation.
The team at The Wilson Firm can help you understand the timeline that may apply to your situation. Reach out for a free case review.
The Legal Process Explained
No. You do not need to file a report with the FDA or complete any special paperwork before speaking with an attorney. In most cases, the best first step is simply gathering information about your injuries, treatment history and the product involved.
During your free case review, our team will examine the details of your situation, including the drug or device involved, your injuries and any medical treatment you received. We may ask questions about timelines, diagnoses and whether you still have medical records or product information available. If we believe you may have a claim, we’ll explain your options, so you can decide how you’d like to move forward.
The Wilson Firm and our trusted partners handle defective drug and device cases on a contingency fee basis. That means there are no upfront costs to hire our firm, and you do not pay attorney fees unless we recover compensation on your behalf.
The timeline for defective drug or device lawsuits varies widely, depending on the complexity of the case, the severity of the injuries and whether the claim is part of larger litigation such as an MDL. Some cases resolve through settlement, while others may take longer if litigation becomes necessary. Our attorneys keep clients informed throughout the process and work to move cases forward as efficiently as possible.
Why Choose Us
Backed by 25 years of legal advocacy, The Wilson Firm LLP has helped families nationwide understand their rights and secure experienced representation across 158 case types.
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If a dangerous drug, defective product or negligent company harmed you or a family member, let us explain legal options that can make your life easier. Case reviews are always free and confidential.