Navilyst Medical Port Catheter Lawsuit [2024 Update]

An Overview of the Navilyst Medical & AngioDynamics Port Catheter Lawsuits

The lawsuits against Navilyst Medical and AngioDynamics center on claims that their port catheter devices are dangerously defective, leading to severe injuries for patients.

Allegations state that the catheters, used for long-term intravenous treatments, are manufactured with an excessive concentration of barium sulfate.

This design flaw causes the devices to degrade over time, leading to cracking, pitting, and increased risks of infection, blood clots, and device fractures.

Plaintiffs argue that the companies failed to adequately test these devices and did not warn patients or healthcare providers of the potential risks.

Medical device manufacturers have a legal and ethical duty to create products that are safe and to provide proper warnings about potential risks.

These lawsuits aim to hold Navilyst Medical and AngioDynamics accountable for the harm their products have caused.

Patients impacted by defective port catheters may be eligible to seek compensation for medical expenses, pain, suffering, and other damages.

TorHoerman Law is actively pursuing justice for those injured by these devices and accepting new clients who have experienced complications.

If you or someone you love has suffered injuries due to a Navilyst Medical or AngioDynamics implantable port catheter device, you may be eligible to file a lawsuit and seek compensation.

Contact us today, or use the chat feature on this page for an instant case evaluation.

Is There a Navilyst Medical Class Action Lawsuit?

No, there is not a class action lawsuit related to catheter fracture, catheter migration, or catheter failure related to the Navilyst Medical or AngioDynamics port catheter device.

Rather, these lawsuits are being consolidated into multidistrict litigation (MDL).

Unlike a class action lawsuit, where one or more plaintiffs represent a larger group of individuals with similar claims, multidistrict litigation (MDL) involves separate individual lawsuits consolidated for pretrial proceedings.

MDL allows each plaintiff to maintain their own case while benefiting from shared evidence and coordinated discovery processes.

This structure is particularly useful in complex product liability cases like the Navilyst Medical and AngioDynamics Port Catheter Lawsuits, where plaintiffs may have suffered different injuries or damages.

While there is no class action for these cases, the MDL process aims to ensure efficiency and consistency in handling shared legal and factual issues, ultimately allowing each plaintiff to pursue their individual claim for compensation.

What is the Bard PowerPort Lawsuit and How is it Similar to This Lawsuit?

The Bard PowerPort Lawsuit involves allegations that the Bard PowerPort device, manufactured by Bard Access Systems, is a defective medical device that has caused severe injuries to patients.

Similar to the Navilyst Medical & AngioDynamics port catheter lawsuits, the Bard PowerPort Litigation focuses on complications arising from implantable port devices used for long-term intravenous treatments like chemotherapy.

Plaintiffs in the Bard PowerPort Litigation claim that the devices are prone to cracking, fracturing, and migrating within the body, leading to serious health risks such as blood clots, infections, and the need for additional surgeries.

Both the Bard PowerPort MDL and the AngioDynamics MDL highlight failures in the design and manufacturing processes of these implantable port devices, as well as insufficient warnings about the potential risks.

While the Bard PowerPort device and the Navilyst Medical port catheter are produced by different companies, the lawsuits share common issues related to material degradation caused by excessive barium sulfate.

In both cases, plaintiffs allege that the high concentration of barium sulfate in the devices’ construction leads to cracking, pitting, and increased susceptibility to infections, blood clots, and fractures.

This material flaw is a central claim in the lawsuits, as it compromises the integrity of these implantable port devices and places patients at significant risk.

These lawsuits underscore the broader accountability of medical device manufacturers to ensure their products are designed with safe, durable materials and thoroughly tested before reaching the market.

Patients injured by either device are seeking compensation for the harm caused and justice for the preventable injuries they have endured.

TorHoerman Law’s team of AngioDynamics/Navilyst Medical and Bard PowerPort Lawyers is accepting new clients for both the Bard Port Catheter Lawsuit and the Navilyst Medical/AngioDynamics Port Catheter Lawsuits.

If you’ve been injured by either a defective Bard PowerPort device or a Navilyst Medical/AngioDynamics port catheter device, contact us today.

How Do Implantable Port Devices Work and Why Are They Used?

Implantable port devices are small, surgically implanted systems designed to provide reliable access to a patient’s vascular system for the delivery of medications, fluids, or other treatments.

These devices are often used in individuals who require long-term, repeated intravenous access, such as those undergoing chemotherapy, long-term antibiotics, blood transfusions, or nutrition therapy.

By offering a more stable and durable alternative to standard IV lines, implantable ports help streamline treatment and minimize the discomfort of frequent needle punctures.

An implantable port device consists of two main components: a port reservoir and a catheter.

• Port Reservoir: The port itself is a small, dome-shaped chamber typically made of metal or plastic. This reservoir is placed just beneath the skin, usually in the chest area. The port is equipped with a self-sealing silicone membrane that allows healthcare professionals to access it with a special needle, known as a Huber needle.
• Catheter: Connected to the port reservoir, the catheter is a thin, flexible tube that is threaded into one of the body’s blood vessels, often a large vein near the heart. This placement ensures that medications, fluids, or blood products are delivered directly into the patient’s vascular system for rapid and effective distribution throughout the body.

Once the device is implanted, the port can be accessed repeatedly without the need for additional punctures in the veins, significantly reducing patient discomfort and preserving the integrity of peripheral veins.

Implantable ports are commonly used in medical settings where reliable long-term access to the bloodstream is necessary.

They offer numerous advantages for patients and healthcare professionals, making treatments safer, more efficient, and less invasive.

Key reasons for using implantable port devices include:

• Repeated Medication Administration: Ports are ideal for chemotherapy, antibiotics, or pain management treatments that require frequent and prolonged intravenous administration.
• Blood Transfusions and Blood Draws: Ports simplify the process of administering blood transfusions or drawing blood for tests, reducing the need for repeated vein punctures.
• Improved Patient Comfort: By eliminating the discomfort of frequent IV insertions, ports enhance the quality of care for patients undergoing long-term treatments.
• Reduced Risk of Vein Damage: Ports protect peripheral veins, which can be damaged or scarred over time due to frequent needle sticks and high-volume infusions.
• Reliable Vascular Access: Ports provide consistent and stable access to the patient’s vascular system, which is particularly beneficial for those with difficult-to-access veins.

Health Complications and Risks Linked to Port Catheter Devices

Port catheter devices, such as those manufactured by Navilyst Medical and Bard Access Systems, are designed to provide long-term intravenous access for treatments like chemotherapy, antibiotics, and nutrition delivery.

However, defects in these devices have been linked to serious and sometimes life-threatening health complications.

Issues such as material degradation, cracking, and migration of the devices have caused significant harm to patients, often requiring additional medical intervention.

Catheter Fracture and Material Degradation

Many port catheter devices, including those implicated in lawsuits, are manufactured using materials containing barium sulfate.

This substance, when used in high concentrations, weakens the catheter structure over time.

As a result, the device may develop cracks, pits, or fractures within the body, creating severe risks for patients.

Key complications linked to catheter fractures include:

• Device Fragmentation: Pieces of the fractured catheter can break off and migrate through the bloodstream, leading to embolisms or blockages in vital organs.
• Bloodstream Infections: The degraded surface of the catheter can harbor bacteria, increasing the risk of sepsis and other life-threatening infections.
• Additional Surgeries: Retrieval of fractured or migrated catheter pieces often requires invasive procedures, which can pose further risks to patients.

Patients may experience pain, swelling, or unusual symptoms at the port site, which could indicate early signs of catheter failure.

If left untreated, these complications can escalate quickly, placing the patient’s health in jeopardy.

Catheter Migration and Improper Functioning

In addition to fracturing, defective port catheter devices are prone to migration, where the device shifts from its original position.

This can result in improper delivery of medication or physical harm to nearby tissues and organs.

Migration can occur due to flaws in the catheter’s design or material degradation.

Risks associated with catheter migration include:

• Medication Delivery Failure: Misplacement of the device may prevent medications or nutrients from reaching the bloodstream effectively, reducing treatment efficacy.
• Organ Damage: Migrated devices can puncture or damage veins, arteries, or surrounding organs, leading to internal bleeding or additional complications.
• Pain and Discomfort: Patients often report pain, swelling, or tenderness around the port site, which can indicate improper positioning.

Catheter migration can significantly disrupt a patient’s treatment plan, often requiring urgent medical intervention to reposition or replace the device.

Severe Infections, Blood Clots, and Related Complications

The rough, cracked surfaces caused by material degradation provide an environment for fibrin accumulation and bacterial growth, increasing the likelihood of infections and blood clots (thrombosis).

These complications are particularly concerning for patients with compromised immune systems, such as those undergoing chemotherapy.

Serious complications tied to infections and blood clots include:

• Sepsis: A life-threatening condition where bacteria enter the bloodstream, potentially causing organ failure.
• Deep Vein Thrombosis: Blood clots can form around the damaged catheter, obstructing veins and increasing the risk of stroke, heart attack, or pulmonary embolism.
• Fibrin Sheath Formation: A build-up of fibrinous material around the catheter can block its functionality and exacerbate the risk of infection.

Patients may experience symptoms such as fever, chills, swelling, or redness at the port site.

Immediate medical attention is often required to address these complications and prevent long-term harm.

The Lasting Impact of Port Catheter Complications

For patients relying on port catheter devices, these complications can be devastating, leading to additional surgeries, prolonged recovery times, and interruptions to critical treatments.

Beyond the physical harm, the emotional and financial toll can be immense, as patients navigate unexpected medical bills, pain, and uncertainty.

Medical device manufacturers have a duty to ensure their products are safe, reliable, and free from preventable defects.

When they fail to meet this standard, patients suffer the consequences.

Lawsuits against Navilyst Medical and AngioDynamics aim to hold these companies accountable for the harm caused by their defective port catheter devices and to provide injured patients with the justice and compensation they deserve.

Do You Qualify for a Navilyst Medical/AngioDynamics Port Lawsuit?

Port catheter injuries can profoundly disrupt a person’s life, causing physical pain, emotional distress, and financial hardship.

The need for additional surgeries, prolonged treatments, and ongoing health concerns can take a significant toll, impacting their ability to work, care for their families, or enjoy daily activities.

These injuries leave individuals not only battling their health but also coping with the uncertainty and frustration of a medical device they trusted failing them.

If you’ve been injured by an implanted port catheter device, you may be eligible to file a lawsuit and seek compensation.

Contact TorHoerman Law today for a free consultation, or use the chat feature on this page to find out if you qualify for a Port Catheter Lawsuit instantly.

Port Catheter Injury Lawyers help clients through the entire legal process, completing the necessary steps of gathering evidence to support the claim and assessing damages to seek compensation that truly reflects the impact of the health complications.

Gathering Evidence for Port-a-Cath Lawsuits

Building a strong case for a port-a-cath lawsuit requires thorough and detailed evidence to demonstrate the connection between the defective device and your injuries.

Collecting the right documentation can support your claim and strengthen your ability to pursue compensation for medical expenses, pain, and suffering.

Evidence in a Navilyst Medical Port Catheter Lawsuit may include:

• Medical Records: Documentation of the implantation procedure, complications, and any additional surgeries required to repair or remove the device.
• Imaging Scans: X-rays, CT scans, or MRIs showing catheter fractures, migration, or other device failures within the body.
• Injury Documentation: Records detailing infections, blood clots, organ damage, or other health complications linked to the defective port-a-cath.
• Device Identification: Information about the port-a-cath manufacturer, model, and serial number to confirm the specific device implanted.
• Treatment Costs: Bills and receipts for medical care, hospital stays, medications, and follow-up procedures related to device failure.
• Personal Testimony: A detailed account of your experiences, including symptoms, treatments, and the impact on your daily life.
• Expert Opinions: Medical expert evaluations linking your injuries to the defective port-a-cath and explaining how the device’s failure caused harm.
• Product Recall Notices: Any documentation or public warnings related to the port-a-cath device that highlight known risks or manufacturing defects.

Damages in Navilyst Medical/AngioDynamics Port Catheter Lawsuits

When defective port catheter devices cause harm, victims may be entitled to seek compensation for the physical, emotional, and financial losses they have endured.

Understanding the types of damages available can help individuals determine the full scope of their claim.

Damages in Port Catheter Lawsuits may include:

• Medical Expenses: Costs for initial implantation, treatment of complications, additional surgeries, hospital stays, medications, and ongoing medical care.
• Lost Wages: Compensation for income lost due to time off work for recovery, medical appointments, or additional surgeries.
• Loss of Earning Capacity: Damages for any long-term or permanent disability that limits your ability to work and earn income in the future.
• Pain and Suffering: Compensation for physical pain, discomfort, and emotional distress caused by device complications and recovery.
• Emotional Distress: Damages for psychological trauma, anxiety, depression, or loss of quality of life related to the injuries and their impact.
• Loss of Consortium: Compensation for the loss of companionship, support, or intimacy experienced by a spouse or family member.
• Out-of-Pocket Expenses: Reimbursement for costs related to travel for medical care, assistive devices, or other expenses tied to treatment and recovery.

TorHoerman Law: Your Port Catheter Injury Lawyer

At TorHoerman Law, we understand the devastating impact that defective port catheter devices can have on your health, your family, and your future.

Our firm is committed to holding manufacturers like Navilyst Medical and AngioDynamics accountable for their negligence and the harm caused by their unsafe devices.

With extensive experience in product liability and medical device litigation, we provide compassionate, personalized representation to help you pursue compensation through this challenging time.

We will fight tirelessly to secure the compensation you deserve for medical expenses, pain and suffering, and the lasting effects of these injuries.

If you or a loved one has suffered complications from a defective port catheter device, contact TorHoerman Law today.

Our team is ready to evaluate your case and help you take the next step toward justice and recovery.

Call us for a free consultation, or use the chat feature on this page for an instant case evaluation.