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Regan Zambri Long’s award-winning Washington, DC defective medical device lawyers represent people whose lives have been changed by unsafe implants and preventable medical technology failures. Over the past 30 years, we have committed our substantial resources and skills to every case, working closely with top medical, engineering, and technical experts to show how a device failed and how that defect affected a patient’s health and future.
We are recognized as one of America’s Best Law Firms, with attorneys who bring deep trial experience to some of the most complex product defect cases in Washington, DC. Our board-certified partners are named among the 500 Leading Plaintiff Consumer Lawyers in the nation, and we have recovered over $1 billion in personal injury awards, including product defect-related outcomes of $15.2 million, $5.5 million, $5 million, $4.2 million, and $3.8 million.
Have you been injured by a defective medical device? Contact Regan Zambri Long today. One of our attorneys will personally call you back, and we’re available 24 hours a day, 7 days a week. We front all case costs, so there’s no fee unless we win your case.
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At Regan Zambri Long, our DC defective products lawyers specialize in handling a wide range of defective medical product cases across Washington, DC. We have extensive experience representing clients injured by medical technologies, including hip and knee implants, cardiac devices like pacemakers and defibrillators, surgical mesh, insulin pumps, glucose sensors, spinal cord stimulators, and diagnostic equipment.
These cases often stem from two primary types of defects: manufacturing defects and design flaws. Manufacturing defects occur during production, where a specific device deviates from its intended design, potentially compromising patient safety. Design flaws represent fundamental problems inherent in the device’s original blueprint that make the entire product line potentially dangerous.
The U.S. Government Accountability Office reports that, out of roughly 200,000 medical devices overseen by the Food and Drug Administration (FDA), nearly 4,000 were recalled between 2020 and 2024, reflecting the ongoing risks posed by defective or unsafe medical technology.
The FDA classifies medical device recalls into three critical levels: Class I (most serious, involving products that could cause serious health problems and even death), Class II (potential temporary health issues), and Class III (least severe, unlikely to cause adverse health consequences).
Understanding these distinctions is extremely important in building a solid legal strategy for defective medical device lawsuits. If you believe a faulty medical device has harmed you, don’t wait—protect your rights and potential compensation. Call an experienced attorney at Regan Zambri Long today at 202-960-4596 for a free, confidential case review.
Identifying potential medical device failures early can be essential to protecting your health and legal rights. Patients should remain vigilant for several key warning signs that may indicate a device is malfunctioning:
If you notice any of these symptoms, immediately document your experiences, stop using the device (if safe), and schedule a comprehensive medical evaluation. Promptly consulting your healthcare provider can help diagnose potential device-related issues and create a critical medical record for legal action.
Do not ignore persistent or worsening symptoms, as they could signal a serious device malfunction that may compromise your health and potentially form the basis of a legal claim. If you’re experiencing device issues, contact a Regan Zambri Long medical device lawyer at 202-960-4596 for a confidential consultation.
Staying informed about potential medical device recalls requires proactive monitoring and utilizing multiple reliable resources. This is especially important given the volume of recalls issued each year. According to Sedgwick’s 2025 U.S. State of the Nation Recall Index, 1,059 medical devices were recalled in 2024 alone, with device failure cited as a leading cause, followed by software problems, mislabeling, and manufacturing defects. The FDA maintains a comprehensive online database of medical device recalls and safety alerts, regularly updated with the most recent safety information about faulty medical devices and medical device companies.
Patients can directly search the FDA’s medical device recall database using their device’s specific model number, manufacturer name, or product code. Additional trusted resources include the manufacturer’s official website, which often posts important safety notices. Medical device safety websites like MedWatch provide real-time updates on potential hazards.
Healthcare providers can also be valuable sources of information, as they typically receive direct notifications about significant device recalls and safety concerns. Medical device manufacturers must legally communicate recall information through multiple channels, including direct patient notifications, healthcare provider alerts, and public announcements. If you’re uncertain about the status of your medical device or suspect a potential issue, don’t hesitate to seek professional guidance.
Victims of defective medical devices are entitled to fair compensation that addresses the full scope of their damages and suffering. Compensation is divided into three categories: economic, non-economic, and punitive.
Economic damages typically encompass:
Non-economic damages can include:
Punitive damages are quite different from economic and non-economic damages. They are also quite rare in a defective medical device lawsuit. These damages are designed to punish the defendant for egregious misconduct and to deter future wrongdoing.
Proving liability requires demonstrating that the medical device manufacturer failed to meet reasonable safety standards through design defects, manufacturing errors, or inadequate warning about potential risks. In Washington, DC, the statute of limitations for medical device claims is typically three years from the date of the injury or its discovery. While this may seem like a long time, if a personal injury claim is not filed within this window, the victim loses all rights to compensation.
Each case requires a nuanced approach, carefully documenting how the defective device directly caused a serious injury and establishing clear causation between the malfunction and the patient’s injuries.
A 2025 analysis of manufacturer reports submitted to the FDA between 2019 and 2022 identified more than 13,500 reports involving patient deaths, over 1.5 million reports of injuries, and nearly 2.9 million reports of device malfunctions. These reports can form a critical evidentiary foundation in defective medical device litigation, helping establish patterns of failure, known risks, and manufacturer knowledge.
The legal team must compile comprehensive medical records, expert testimony, and detailed evidence to build a compelling case that substantiates the full extent of the client’s damages. Time is of the essence in these complex legal matters. If you’re concerned about your rights and potential compensation, call the dedicated medical device attorneys at Regan Zambri Long at 202-960-4596 for a free consultation.
Several parties may share liability for your injuries depending on the circumstances and the device involved. These may include:
Depending on the circumstances, the verdicts and settlements for defective medical device claims may be large since victims often need medical assistance for the rest of their lives. A medical device lawyer from our firm can identify all potentially liable parties on your behalf and help you file a product liability lawsuit.
Navigating a product liability claim requires a strategic and comprehensive legal approach tailored to each unique defective medical device case. The process typically begins with an initial confidential consultation, where a DC defective medical device attorney meticulously reviews medical records, device history, and potential evidence of manufacturer negligence.
Our legal team conducts thorough investigations, gathering expert medical testimony, technical device analysis, and comprehensive documentation to build a compelling case. Most medical device claims are handled on a contingency fee basis, meaning clients pay no upfront legal fees, and our attorneys are compensated only if we win your case. The legal journey may involve negotiating with device manufacturers and their insurance companies, filing detailed legal documents, and potentially pursuing litigation if a fair settlement cannot be reached.
Emergency procedures may be implemented for cases involving immediate health risks, allowing for expedited legal action and potential temporary injunctive relief. Our attorneys communicate constantly throughout the process, ensuring clients understand each stage of their legal proceedings and possible outcomes. Complex medical device claims can take months or even years to resolve, depending on the specific circumstances and complexity of the case. Our lawyers are ready and willing to take on the fight. Contact Regan Zambri Long today to learn how we can help.
At Regan Zambri Long, our commitment to medical device injury victims sets us apart. With nearly 200 years of combined legal experience and a proven track record of securing multi-million dollar settlements, our dedicated team has successfully recovered over $1 billion for injured clients, including awards relating to defective products such as:
We serve Washington, DC, and the surrounding areas, providing comprehensive legal representation for complex medical device claims. Available 24/7, our attorneys offer personalized attention and aggressive advocacy, ensuring each client receives the highest-quality legal support.
Recognized by prestigious legal organizations and consistently ranked among the top personal injury firms, we’re prepared to fight tirelessly for your rights.
That level of advocacy is backed by credentials that matter in high-stakes cases involving technical evidence and serious injuries. All three founding partners are AV Preeminent rated by Martindale-Hubbell, the highest peer-reviewed rating for legal ability and ethics, and board certified in Civil Trial Law and Civil Trial Advocacy by the National Board of Trial Advocacy, a distinction held by about 4% of U.S. lawyers.
Our attorneys are also deeply rooted in Washington, DC trial practice and leadership. The founding partners, along with partner Paul Cornoni, have each served as President of the District of Columbia Trial Lawyers Association, while partners Jacqueline Colclough and Christopher Regan currently sit on the Association’s Board of Governors. Patrick Regan also sits on the Board of Governors of the American Association of Justice, and Salvatore Zambri serves as the National Board Representative for the DC chapter of the American Board of Trial Advocates. Victor Long is the Chair of the Washington, DC Court of Appeals Client Security Trust Fund, reflecting trusted service in the legal community at the highest levels.
Best Lawyers has consistently named Regan Zambri Long as one of the Best Law Firms in America, and has also recognized Patrick Regan as Lawyer of the Year for Mass Tort Litigation twice and Medical Malpractice Law, Salvatore Zambri for Product Liability Litigation, and Paul Cornoni for Workers’ Compensation and Personal Injury Litigation. Paul was also honored with the District of Columbia Bar Association’s 2025 Pro Bono Attorney of the Year award for his work on behalf of the District’s most vulnerable residents.
Put our extensive experience to work for you—contact Regan Zambri Long at 202-960-4596 today.
In Washington, DC, medical devices are classified as defective when design flaws, manufacturing errors, or insufficient warnings/instructions lead to patient harm. These defects may violate FDA standards or federal safety regulations.
A defective device can malfunction during use, deliver incorrect treatment, or fail to operate as intended. Such failures may worsen health conditions, surgical complications, or long-term disability.
Common injuries include infections, internal bleeding, organ damage, nerve injury, and device migration or breakage. Some patients may also suffer from chronic pain or require additional surgeries to correct the issue.
Examples of unsafe or defective medical equipment include malfunctioning pacemakers, hip or knee implants that break or wear prematurely, faulty surgical mesh, and insulin pumps that misdose medication—many of which have been subject to recalls in DC and nationwide.
In Washington, DC, a wrongful death claim may be filed against the manufacturer, distributor, or healthcare provider. Families can seek compensation for medical costs, pain and suffering, funeral expenses, and loss of companionship.
Have you or your loved one sustained injuries in Washington DC, Maryland or Virginia? Regan Zambri Long PLLC has the best lawyers in the country to analyze your case and answer the questions you may have.