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McGuire Law

Columbia Defective Medical Devices Personal Injury Lawyer

When medical devices fail inside your body, the consequences can be catastrophic, requiring emergency surgeries, permanent disability, or even threatening your life. Columbia, South Carolina patients trust that implanted devices like hip replacements, pacemakers, and surgical mesh will improve their health, not cause additional suffering through design flaws or manufacturing defects.

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Available 24/7 - Immediate Response for Medical Device Injury Cases

Attorney Matt McGuire

Whether you're experiencing pain from a faulty hip implant, infections from contaminated surgical instruments, or device malfunctions that require repeated surgeries, immediate legal action is essential to preserve evidence and hold manufacturers accountable. Matthew M. McGuire has dedicated over 30 years to fighting for patients harmed by defective medical devices, understanding how these complex cases require extensive medical expertise and resources to challenge powerful device manufacturers who prioritize profits over patient safety throughout South Carolina.

With offices in Columbia and availability 24/7/365, McGuire Law responds immediately when device failures occur—because in medical device cases, preserving evidence and documenting injuries quickly is critical for building your case against well-funded manufacturers.

The Legal Expertise of McGuire Law

Medical device litigation demands specialized knowledge of FDA regulations, product liability law, and complex medical evidence. Our decades of experience navigating these intricate cases gives Columbia patients the skilled representation they need against well-resourced device manufacturers.

Trial Experience

While many device cases settle through mass tort litigation, we're always prepared for trial. Our courtroom experience gives us leverage in negotiations and confidence when litigation is necessary to secure maximum compensation for device injuries.

Federal Court Practice

Admitted to practice in federal courts with extensive experience handling complex medical device litigation. Federal device cases require specialized knowledge of preemption defenses and federal regulatory frameworks.

Discovery and Investigation

Thorough investigation and discovery practices uncover manufacturer knowledge of device dangers, concealed safety data, and regulatory violations that prove negligence and strengthen your claim.

Expert Witness Coordination

Extensive network of expert witnesses including biomedical engineers, orthopedic surgeons, cardiologists, and FDA regulatory specialists. Expert testimony often makes the difference in proving device defects caused your injuries.

Motion Practice Excellence

Skilled at drafting and arguing motions to overcome manufacturer preemption defenses, compel document production, and exclude improper expert testimony. Strong motion practice resolves critical issues before trial.

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Common Defective Medical Device Categories

Medical device failures affect patients across Columbia through design defects, manufacturing problems, and inadequate safety warnings. Understanding these categories helps identify your potential claim.

Orthopedic Implants

Hip replacements, knee implants, and spinal fusion devices that fail prematurely, causing bone damage and requiring revision surgeries with extended recovery periods.

Cardiovascular Devices

Pacemakers, defibrillators, and stents that malfunction, leading to heart attacks, strokes, or sudden cardiac death requiring emergency intervention.

Surgical Mesh Products

Hernia repairs and pelvic organ prolapse mesh that erode, migrate, or cause severe infections requiring emergency removal and ongoing complications.

Transvaginal Mesh

Implants causing chronic pain, organ perforation, and sexual dysfunction affecting women throughout Columbia who trusted these devices for pelvic support.

IVC Filters

Blood clot prevention filters that break apart, migrate to vital organs, or fail to be retrievable when needed, causing life-threatening complications.

Breast Implants

Devices that rupture, leak, or cause rare cancers, requiring multiple surgeries and extensive medical treatment for affected patients.

Insulin Pumps

Devices delivering incorrect dosages or failing to alert diabetic patients to dangerous blood sugar levels, causing severe medical emergencies.

Device Recalls Affect Thousands of Patients

When manufacturers recall defective devices, patients who already have them implanted face difficult decisions about removal, monitoring, or revision surgeries.

McGuire Law's Core Values

Patients harmed by defective medical devices deserve attorneys who combine compassionate understanding with aggressive advocacy against powerful manufacturers. Our values ensure you receive personalized attention while we fight for maximum compensation.

Client-Centered Service

Your device injury case is not just another file to us. We take time to understand your specific injuries, medical needs, and how the device failure has impacted your life and family.

Aggressive Advocacy

We fight hard against well-funded device manufacturers. Whether challenging FDA approval processes, subpoenaing internal documents, or presenting your case to a jury, we advocate aggressively for your rights.

Thorough Case Preparation

We prepare every device case as if it's going to trial, even those likely to settle through mass tort litigation. This preparation gives us leverage in negotiations and confidence in court.

Attention to Detail

Medical device cases are won and lost on technical details. We meticulously review every FDA filing, engineering specification, and clinical trial result to build the strongest possible case.

Client Empowerment

We empower clients by explaining complex device litigation, your legal options, and settlement decisions in plain language. Your case, your choice—with expert guidance every step of the way.

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Immediate Post-Device Failure Response Protocol

When medical devices fail, taking the right steps immediately protects your health, preserves evidence, and strengthens your legal claim against manufacturers.

Seek Emergency Medical Care

Get immediate treatment at Prisma Health Richland Hospital or other Columbia medical facilities if experiencing sudden device-related symptoms or complications.

Preserve All Documentation

Save all device packaging, patient identification cards, and medical records documenting the original implantation or device placement procedure.

Obtain Device Information

Request the device's lot number, serial number, and manufacturer information that may be crucial for identifying defective product batches.

Document Your Symptoms

Record symptoms, pain levels, and functional limitations through detailed written records and photographs when appropriate to establish the timeline.

Report to FDA MedWatch

File reports with the FDA's MedWatch program while preserving evidence for potential legal action against the device manufacturer.

Contact McGuire Law Immediately

Call (888) 499-5738 before speaking with device company representatives who may attempt damage control and minimize your claim.

The McGuire Law Difference

Taking on medical device manufacturers requires attorneys who understand product liability law, FDA regulations, and complex medical evidence. Matt McGuire has fought these corporate giants for over 30 years, securing compensation for patients harmed by devices that should have protected their health.

Personal Attention, Not Assembly Line Service

At McGuire Law, you're not just a case number in a mass tort database. You're a person facing serious health consequences from a device failure, and you deserve an attorney who treats your case with individual attention.

Same-Day Response Guarantee

When you're dealing with device complications, every hour counts for preserving evidence. We guarantee same-day response to all device injury inquiries—even on weekends and holidays.

Always Accessible

When you need us, we're there. Our attorneys are responsive, available, and committed to keeping you informed about your device litigation and settlement negotiations every step of the way.

Results-Driven Representation

We're focused on outcomes that matter—securing compensation for medical expenses, lost wages, pain and suffering, and future care needs resulting from defective device injuries.

Clear Communication, No Legal Jargon

We explain complex device litigation, FDA regulatory issues, and settlement terms in plain language so you can make informed decisions about your case with confidence.

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Comprehensive Damage Assessment and Recovery Options

Device failure victims deserve full compensation for all the ways their injuries have affected their lives, families, and futures.

Economic Damages

  • Medical expenses covering emergency treatments, device removal surgeries, and revision procedures
  • Lost wages for extended recovery periods and multiple surgeries
  • Future medical care costs including lifetime monitoring and potential revisions
  • Disability accommodations and assistive equipment for permanent impairments

Non-Economic Damages

  • Pain and suffering for chronic discomfort and emotional trauma
  • Loss of consortium for spouses affected by device-related limitations
  • Punitive damages when manufacturers concealed known dangers
  • Wrongful death compensation for families who lost loved ones

Mass Tort Litigation Can Strengthen Your Claim

Coordinating with national litigation teams handling similar device injury claims increases resources and leverage against manufacturers.

FDA Oversight Failures and Manufacturer Accountability

We investigate every aspect of how defective devices reached the market and why manufacturers failed to protect patient safety.

510(k) Clearance Investigation

Examining FDA approval processes that allowed dangerous devices to reach market without adequate safety testing based on claimed similarity to older products.

Post-Market Surveillance Analysis

Reviewing clinical trial data and surveillance reports that may reveal known safety problems manufacturers failed to address or report.

Internal Document Subpoenas

Compelling production of internal company documents including design specifications, safety testing results, and marketing strategies that prioritize profits over safety.

Quality Control Review

Examining manufacturer quality control procedures and inspecting facilities where defective devices were produced under inadequate oversight.

Regulatory Expert Coordination

Working with former FDA officials and industry insiders who can testify about regulatory failures and manufacturer misconduct in device approvals.

Frequently Asked Questions

Patients facing device injury litigation have important questions about their rights, the legal process, and what compensation they may be entitled to receive.

What should I do if my medical device fails?

Seek immediate medical attention, preserve all device packaging and documentation, obtain the device serial number, and contact an experienced device injury attorney before speaking with manufacturer representatives.

How long do I have to file a device injury claim?

South Carolina's statute of limitations varies depending on when device complications were discovered or should have been discovered. Contact us immediately to ensure you don't miss critical deadlines.

Can I sue if my device was FDA approved?

Yes. FDA approval doesn't shield manufacturers from liability for design defects, manufacturing problems, or failure to warn about known risks. We navigate complex preemption defenses to hold manufacturers accountable.

What is mass tort litigation?

Mass tort litigation coordinates claims from multiple patients injured by the same defective device, increasing resources and leverage against manufacturers while maintaining your individual case.

Should I have my device removed?

This is a medical decision that should be made with your doctors. We can help coordinate with medical experts to ensure proper documentation of the device and your injuries for your legal claim.

What compensation can I receive?

Compensation may include medical expenses, lost wages, pain and suffering, future care costs, and punitive damages when manufacturers acted with reckless disregard for patient safety.

How long do device injury cases take?

Device cases typically take 1-3 years depending on complexity, coordination with national litigation, and settlement negotiations. We push aggressively for resolution while protecting your rights.

What does device injury representation cost?

Most device injury cases are handled on a contingency fee basis—you pay nothing unless we recover compensation for you. Call for free to discuss your case and understand your options.

Matt McGuire - Attorney

About South Carolina Attorney Matt McGuire

Matt McGuire South Carolina Criminal Defense Personal Injury Family Law Attorney

With over 30 years of experience defending South Carolina, McGuire Law provides elite legal representation with national recognition. McGuire Law has grown from a small practice into one of the most trusted law firms in South Carolina. We understand that legal issues can be overwhelming, whether you're facing criminal charges, dealing with injuries from an accident, or navigating family law matters.

McGuire Law is committed to each client's unique situation, and we don't believe in boilerplate solutions. Every case requires careful analysis, strategic planning, and aggressive representation. Our firm combines over 30 years of experience with cutting-edge legal strategies to achieve the best possible outcomes for our clients.

McGuire Law serves all 46 South Carolina counties. We know these counties, their courts, their legal communities, and most importantly, the people who live here. This local knowledge, combined with our legal expertise, gives our clients a significant advantage.

Matt McGuire received his B.A. from the University of North Carolina - Chapel Hill and his J.D. from the University of South Carolina.

Matt has served as a law clerk for a State Circuit Judge, an Assistant Attorney General for the State of South Carolina, and an Assistant Solicitor in the Fifth Circuit Solicitor's Office.

Matt is a proud husband, father of two, and a long-time resident of Richland County, South Carolina.

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Get Started Today

When defective medical devices have caused you serious injury, you need more than just any attorney – you need Matt McGuire and McGuire Law.

Don't let another day pass without proper legal protection against device manufacturers who prioritized profits over your safety. Call McGuire Law now and experience the difference that personal, aggressive, and effective legal representation can make in your device injury case.

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Columbia Office

2001 Assembly Street, Suite 102-B
Columbia, SC 29201

(888) 499-5738

Contact McGuire Law Today

Don't suffer in silence while defective medical device manufacturers escape responsibility for their dangerous products – call (888) 499-5738 now for immediate consultation about your case. Matt McGuire's three decades of experience taking on powerful medical device companies and 24/7 availability ensure you get the tenacious advocacy needed to secure maximum compensation.

"The arc of the moral universe is long, but it bends toward justice." — Theodore Parker