Fighting for Those Injured by Defective Medical Devices

With decades of combined legal experience, our attorneys have recovered millions of dollars in verdicts and settlements for our clients, proving our commitment to pursuing justice at every turn. Our founding attorney, Mike “’Maggio” Saltaformaggio, has been recognized by The National Trial Lawyers Top 40 Under 40, The National Trial Lawyers Top 25 Motor Vehicle Accident Attorneys, and the American Institute of Personal Injury Attorneys’ Top 10 list.

We leverage our extensive trial experience, resources, and professional network to hold big corporations accountable for defective medical devices. We’re here to help secure the compensation and peace of mind our clients need to rebuild their lives. Contact us today.

Why Your Case Matters

When a company manufactures a medical device, it is responsible for ensuring that the product is safe and effective.

By filing a lawsuit, you will defend your right to fair compensation and help drive awareness and accountability for potentially hazardous medical products.

It’s about protecting your health and financial stability—and potentially sparing others from the same harm [Product Liability Law, Restatement (Third) of Torts].

The Danger of Defective Port Catheters

Port catheters—often used for administering medications, chemotherapy, or nutritional support—are intended to make treatment more manageable and comfortable. Unfortunately, some of these devices are prone to breakage, infection, or other failures, putting patients at serious risk.

Potential complications may include:

  • Device fracture or breakage
  • Infection at the port site
  • Blood clots or thrombosis
  • Catheter migration or perforation
  • Pain, swelling, and tissue damage
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Alleged Defects & Potential Injuries

Several lawsuits claim that AngioDynamics port catheters can fracture, migrate, or otherwise malfunction, possibly leading to:

  • Infections & Sepsis: If the catheter or implant site becomes contaminated, it can lead to severe, sometimes life-threatening infections [FDA Guidance on Infection Control, 2023].
  • Device Fracture or Breakage: Broken or cracked components can cause internal damage, bleeding, and the need for additional surgeries to remove or replace the device [AngioDynamics 2022 Annual Report].


These complications may require surgeries, hospitalizations, and prolonged medical care, disrupting a patient’s life, both physically and financially.

AngioDynamics, Inc. Port Catheter Lawsuit

AngioDynamics, Inc. port catheters are designed to help patients receive critical treatments such as chemotherapy or nutrition with fewer needle sticks. Unfortunately, these devices may fail due to alleged design and manufacturing defects, exposing patients to serious health complications.

As a result, individuals harmed by defective AngioDynamics port catheters are taking legal action to hold the company accountable for its negligence [see FDA Medical Device Reports, Manufacturer and User Facility Device Experience (MAUDE) Database].

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Legal Claims Against AngioDynamics

Patients who have filed claims allege:

  1. Defective Design: The port catheters were not properly engineered to withstand typical use, making them prone to breakage or leakage [AngioDynamics 510(k) Premarket Notification Summaries].
  2. Manufacturing Errors: Poor quality control during production resulted in flaws that put patients’ health at serious risk.
  3. Failure to Warn: AngioDynamics neglected to provide adequate warnings or instructions about the risks, preventing patients and healthcare providers from making informed decisions [FDA Warning Letters].
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Navilyst Inc. Port Catheter Lawsuit

Navilyst Inc. port catheters, commonly used to administer chemotherapy, intravenous fluids, and other critical treatments, have come under scrutiny due to allegations of design and manufacturing defects. These concerns center on reports of device failure that can lead to severe medical complications, triggering a wave of product liability lawsuits against the company.

Reported Complications & Alleged Defects

  • Catheter Fractures or Cracks
    • Impact on Patients: When a catheter fractures, pieces may migrate into blood vessels or surrounding tissue, causing intense pain, bleeding, or even blockages.
    • Evidence: Patients and healthcare professionals have reported incidents of broken or cracked Navilyst catheters to the FDA’s MAUDE Database [FDA MAUDE Database – Navilyst Search].
  • Migration or Dislodgement
    • Impact on Patients: A dislodged port or catheter piece can perforate veins, cause vascular injury, or travel to other parts of the body, leading to life-threatening complications.
    • Evidence: Court records highlight instances in which unexpected catheter movement has allegedly resulted in the need for emergency surgery and extended hospital stays [Navilyst Product Liability Filings – Justia].
  • Infection Risks
    • Impact on Patients: Infections at the insertion site—or systemically—may occur if the integrity of the catheter is compromised or if manufacturing processes don’t meet safety standards.
    • Evidence: Adverse event reports submitted to federal agencies cite concerns over infection complications potentially linked to port malfunctions [FDA Enforcement Reports – Navilyst Medical, Inc.].

Legal Grounds for Claims Against Navilyst Inc.

Individuals who have filed lawsuits against Navilyst Inc. often base their claims on the following legal theories:

  • Defective Design: Plaintiffs argue that Navilyst port catheters contain inherent flaws in their design, rendering them unfit for safe use and significantly increasing the risk of fractures or migration.
  • Manufacturing Defects: Lawsuits contend that quality control processes at Navilyst Inc. were insufficient, leading to inconsistencies in product integrity and a greater chance of device failure.
  • Failure to Warn: Claimants allege that Navilyst neglected to provide adequate risk information or instructions, leaving patients and healthcare providers unaware of serious potential hazards before consenting to use these devices.

Potential Damages for Affected Patients

If you have suffered complications from a Navilyst Inc. port catheter, you may be entitled to compensation for:

  • Medical Expenses: Including hospital stays, surgeries, and ongoing treatments resulting from the defective device.
  • Lost Wages & Earning Capacity: Covering work missed during recovery and any long-term impact on your ability to earn an income.
  • Pain & Suffering: Accounting for the physical pain, emotional distress, and reduced quality of life caused by your injuries.
  • Punitive Damages: In some cases, courts may award punitive damages to penalize a company for especially negligent or reckless conduct.
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The ‘Maggio Process: How We Fight for You

Comprehensive Evaluation

We start by assessing every aspect of your case, including your medical history, the product’s usage, and the timeline of your injuries. Our attorneys consult medical experts to confirm that the device’s failure caused or contributed to your harm.

In-Depth Investigation

We diligently review company documents, analyze product design and manufacturing processes, and investigate similar claims to establish patterns of negligence.

Aggressive Advocacy

Armed with evidence, we build a compelling argument that demonstrates the defendant’s liability. If settlement talks fail to yield fair compensation, we stand ready to take your case to court and fight for your right to a just recovery.

Client-Centered Representation

Personalized, caring service is as vital as winning results. Our promise is to keep you informed at every step, return your calls the same day, and guide you through the legal process.

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Why ’Maggio Law?

  1. Personalized Representation: At ’Maggio Law, we believe in a one-on-one approach. You won’t be shuffled off to a paralegal or assistant. Every case we take on is handled by a dedicated attorney who truly cares about your well-being and future.
  2. Experience & Compassion: With decades of combined experience, our legal team has successfully taken on large corporations and insurance companies—and won. Our deep roots in Mississippi keep us connected to our community, and we work tirelessly to protect the rights of those who need it most.
  3. No Fees Unless We Win: Facing medical expenses and lost income can be overwhelming. That’s why we work on a contingency fee basis, meaning we don’t get paid unless we secure a settlement or verdict for you. Your financial security is our top priority.

We’re on Your Side

Medical device manufacturers must be held accountable when they place profits over patient safety. At Maggio Law, our mission is to stand up for the rights of individuals harmed by defective products. We understand how life-altering these injuries can be, and we’re here to shoulder the burden so you can focus on what truly matters—your health and recovery.

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FAQ

How can I find out if my port catheter is an AngioDynamics or Navilyst device?

Most port catheters have identifying information—such as a model name or number—printed on the patient implant card you received after surgery. If you don’t have that card, you can request a copy of your surgical or implant records from your healthcare provider or hospital. Those records should indicate both the manufacturer and model of the device.

Is there a statute of limitations for filing a lawsuit related to defective port catheters?

Yes. Each state has its own statute of limitations, meaning you have a limited time to file a product liability lawsuit. The clock generally starts when you either knew—or should have reasonably known—that your injuries were linked to the defective catheter. An attorney can help determine the exact deadline based on your state’s laws.

What if my catheter was removed or replaced, and I no longer have it?

Even if the device itself is no longer in your body, you may still have a viable claim. Medical records, imaging scans, surgical notes, and pathology reports can often provide sufficient evidence of the device’s failure and how it harmed you. It’s important to preserve any documentation you have or can obtain from your healthcare providers.

Do I need an official recall notice to pursue legal action?

Not necessarily. A device does not have to be recalled for you to file a lawsuit. If you can show that your AngioDynamics or Navilyst port catheter was defective and caused you harm, you may be able to pursue compensation. However, if a recall does exist, it can serve as additional evidence in your case.

Can I still file a claim if I haven’t had surgery to remove or fix my port catheter?

Yes. If you are experiencing complications or symptoms, you do not necessarily need corrective surgery before seeking legal help. In many cases, medical evaluations and expert opinions on the nature of your device failure are enough to support a lawsuit. An attorney can help guide you on next steps if removal is recommended by your physician.

What if I have preexisting health conditions—can that affect my claim?

Preexisting conditions don’t automatically bar you from recovering damages. In fact, a defective catheter can exacerbate existing health issues or create additional complications. Courts typically look at whether the device failure aggravated or worsened your health beyond what your preexisting condition would have caused on its own.

Are these cases handled individually or as part of a larger group, such as a class action or multidistrict litigation (MDL)?

It varies. While some product liability cases may be centralized under MDL for pretrial proceedings (to streamline discovery and motions), each claim is typically litigated on its individual merits. This means that even in an MDL, each plaintiff’s injury and damages will be evaluated separately. Consulting with an attorney can clarify whether your claim is best handled individually or in a consolidated process.

Contact ’Maggio Law

Call us or reach out online to schedule a free, no-obligation consultation. We’re here 24/7, and we’re ready to help you pursue justice against corporations that put you in harm’s way.

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