AngioDynamics Port Catheter Lawsuits

Fighting for Victims Nationwide

Robert Peirce & Associates, P.C. is investigating potential claims from patients who suffered injuries involving defective AngioDynamics port catheters. These implantable medical devices, used for long-term vascular access in patients requiring frequent medication delivery or transfusions, have been linked to serious complications and adverse health effects.

Manufactured by AngioDynamics, these port catheters are now the subject of growing litigation from victims who claim they endured injuries that were not fully disclosed by the manufacturer. Plaintiffs allege that defects in these devices have led to severe complications, including infections, blood clots, and catheter fractures, potentially resulting in life-threatening conditions.

If you or someone you love experienced complications after receiving an AngioDynamics port catheter implant – such as an infection, fracture, or catheter migration – you may have a case. Call (844) 383-0565 or contact us online for a FREE consultation.

Why Choose Us?

Robert Peirce & Associates, P.C. is a nationally recognized trial practice known for handling complex and high-stakes personal injury cases across the country. Led by award-winning trial lawyers, we’ve amassed extensive experience litigating cases involving defective medical devices and product liability. 

Reasons why we’re trusted by clients and colleagues include:

• Millions of dollars in verdicts and settlements.
• Proven results against powerful defendants and corporations.
• Decades of collective legal experience. 
• Personalized, one-on-one attention.

Learn more about our team, our high-profile work, and what clients have to say about working with us. 

Do I Have an AngioDynamics Port Catheter Lawsuit?

You may have grounds to file a lawsuit if you or a loved one:

• Had an AngioDynamics port-a-catheter implanted at any time after 1996, and
• Experienced serious complications within five years of implantation, such as:
  • Catheter fracture or device breakage
  • Migration of broken catheter fragments
  • Catheter-related bloodstream infections or sepsis
  • Thrombosis or other vascular complications
  • Dislodgement of the catheter from the implanted port
  • Organ perforation or embolism
  • Death resulting from port-related complications

These injuries can cause immense harm, often requiring hospitalization, emergency surgery, or long-term medical care. In some cases, they have proven fatal. Lawsuits allege that these risks stem from defective materials — particularly excessive barium sulfate in the catheter — and AngioDynamics' failure to adequately warn doctors and patients.

If you or a family member suffered any of the above complications, you may be eligible to pursue legal action. Our attorneys are actively investigating these claims and can review your case during a free, confidential consultation.

What Are AngioDynamics Port Catheters?

AngioDynamics port catheters are implantable vascular access devices used to deliver medication, chemotherapy, and other intravenous treatments directly into the bloodstream. These devices typically consist of a small reservoir implanted under the skin and a catheter that connects to a major blood vessel.

AngioDynamics port catheters are marketed as long-term solutions for patients needing frequent intravenous therapy, reducing the need for repeated needle sticks. However, concerns have emerged regarding their safety, as numerous patients have reported experiencing severe side effects, leading to lawsuits against the manufacturer.

AngioDynamics and its subsidiary, Navilyst Medical, produce various port catheters, including devices marketed under its SmartPort Series and Vortex Series.

• SmartPort: Smart Port CT, Smart Port LP, SmartPort MP
• Vortex: Vortex LP, Vortex MP, Vortex TR, Vortex VX

Other AngioDynamics devices that may be defective include the BioFlo Port Catheter, Xcela Plus Port Catheter, and Navilyst PowerPort.

Complications Linked to AngioDynamics Port Catheters

Patients and medical professionals have reported a variety of serious complications linked to AngioDynamics port catheters, including:

• Infections, including sepsis
• Blood clots and deep vein thrombosis (DVT)
• Catheter fractures leading to migration of broken pieces
• Pulmonary embolism
• Perforation of veins, organs, or other tissues
• Cardiac arrhythmias
• Chronic and severe pain
• Necrosis and tissue damage at the implantation site

These complications often require emergency medical intervention, surgical removal of the device, and extended hospitalization, increasing the burden on affected patients and their families. They have also been implicated in several recalls, including:

• FDA Recall 1: SmartPort Recall (February 22, 2021) – AngioDynamics recalled certain SmartPort kits due to sterility concerns, which posed a heightened risk of infection for vulnerable patients. The FDA classified this as a Class I recall, the most serious type, indicating a potential for severe injury or death.
• FDA Recall 2: Vortex MP Port Recall (September 20, 2022) – AngioDynamics recalled the Vortex MP Port system due to labeling issues. The labels failed to disclose the presence of Di(2-ethylhexyl) phthalate (DEHP), a chemical associated with cancer and reproductive harm.

Lawsuits Allege Defective Design, Negligence

Lawsuits filed against AngioDynamics and its subsidiary Navilyst Medical allege that the company failed to properly design, test, and warn about the risks associated with its port catheter devices. Claims against the manufacturer include:

• Defective design that makes the catheter prone to breaking, fracturing, or migrating within the body.
• Failure to warn patients and physicians about the potential risks and complications.
• Negligent manufacturing processes, including manufacturing the port catheters with excess barium sulfate, that resulted in improper material composition, making the device more susceptible to wear and degradation.
• Failure to conduct adequate clinical testing before releasing the product onto the market.

As with the Bard PowerPort litigation, AngioDynamics Port Catheter lawsuits have been consolidated before a single federal court through a process known as multidistrict litigation (MDL), which allows federal courts to streamline pretrial proceedings for similar claims filed across the country. The AngioDynamics MDL (MDL No. 3125) is being handled in United States District Court for the Southern District of California and includes a growing number of claims.

Compensation for AngioDynamics Port Catheter Injury Lawsuits

Victims who pursue legal claims against AngioDynamics may be entitled to financial compensation for their injuries, including:

• Medical expenses, including hospital stays, surgeries, and rehabilitation
• Lost wages due to inability to work during recovery
• Pain and suffering from physical and emotional distress
• Long-term disability costs
• Wrongful death damages for families who lost a loved one due to complications

Compensation varies depending on the severity of injuries and the circumstances surrounding each case, but legal action can help hold the manufacturer accountable and provide financial relief for victims and their families.

If any of these complications happened to you or your loved one, our attorneys want to hear your story. Call (844) 383-0565 for a free, confidential consultation.

Frequently Asked Questions (FAQs)

How Do I Pursue a Claim?

If you believe you have suffered injuries due to an AngioDynamics port catheter, start by gathering your medical records, including details about your implant, complications, and any corrective procedures. Contact Robert Peirce & Associates, P.C. for a free consultation, where we will review your case and determine your eligibility for legal action. If qualified, you may join a mass tort lawsuit alongside other affected patients.

How Do I Know If I'm Eligible to File a Claim?

You may qualify to file a claim if you experienced serious complications from an AngioDynamics port catheter, such as infection, blood clots, catheter fracture, or migration. If your injuries required additional surgeries, hospitalizations, or medical treatments, you may have grounds for legal action.

What Are the Allegations Against AngioDynamics?

Lawsuits allege that AngioDynamics failed to properly design, manufacture, and warn patients and healthcare providers about the risks of their port catheters. Plaintiffs claim the devices are prone to fracturing, migrating, or causing severe infections, leading to serious health complications.

What Evidence Do I Need for My Case?

To strengthen your claim, you should collect medical records related to your catheter implant and any subsequent complications, documentation of additional treatments or surgeries, and any communications with your healthcare providers regarding issues with the device. Our legal team can help gather the necessary evidence to support your case.

Are There Any Recalls Related to AngioDynamics Port Catheters?

Yes. AngioDynamics has issued multiple recalls due to concerns about sterility, labeling issues, and risks of severe infections or exposure to harmful chemicals. These recalls strengthen claims that the company failed to ensure the safety of its products.

What Is the Legal Process for Filing a Claim?

The legal process typically involves an initial case evaluation, gathering evidence, filing a lawsuit, and potentially joining mass tort litigation. If your case proceeds, our attorneys will negotiate for a settlement or take your claim to trial if necessary.

How Long Do I Have to File a Lawsuit?

The statute of limitations for filing a defective medical device claim varies by state. It is important to act quickly, as missing the deadline could prevent you from recovering compensation. Contact us as soon as possible to determine your eligibility.

Call for a FREE Consultation: (844) 383-0565

Robert Peirce & Associates, P.C. is a nationally recognized trial law firm with a history of success in defective medical device litigation. Our team has the experience and resources needed to hold major corporations accountable and recover compensation for victims of faulty port catheter devices.

If you have suffered injuries due to an AngioDynamics port catheter, don’t wait to explore your legal options. Call (844) 383-0565 or contact us online for a FREE consultation. Our firm serves clients nationwide and operates on a contingency basis, meaning there’s no fees unless we win your case.