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Bard PowerPort Lawsuit [April 2025 Update] - File A Claim

TorHoerman Law is helping injured patients join the Bard PowerPort Lawsuit.

Contact us today for a free consultation, or use the chat feature on this page to find out if you're eligible to file a Bard PowerPort Lawsuit.

  • Last Updated: April 14th, 2025

Key takeaways:

  • The Bard PowerPort Lawsuit involves claims that certain Bard PowerPort implantable port catheter devices are prone to fracturing, migrating, or causing infection, leading to serious health complications.

  • Lawsuits allege that Bard Access Systems Inc. and Becton Dickinson failed to adequately warn patients and healthcare providers of these risks.

  • The Bard PowerPort Lawsuit is ongoing with over 1,200 cases consolidated in the Bard Implanted Port Catheter Products Liability Litigation (MDL 3081).

Most Recent Updates:

  • More than 1,200 Bard PowerPort Lawsuits are pending in the federal MDL.

  • Claims involving the Bard Power Port devices focus on serious health issues allegedly caused by design and manufacturing defects.

  • Contact us today for a free consultation or use the chatbot on this page to find out if you qualify for the Bard PowerPort Lawsuit instantly.

Our Attorneys Can Help You File a Bard PowerPort Lawsuit

This page is intended for individuals seeking information about the Bard PowerPort Lawsuit, including current updates, eligibility, and potential compensation for injuries linked to the Bard PowerPort implantable port catheter device.

TorHoerman Law’s team of Bard PowerPort Lawyers are actively accepting new clients and helping them join the ongoing Bard PowerPort Litigation.

On this page, we’ll provide an overview of the Bard PowerPort Lawsuit, technical issues and injuries associated with the Bard PowerPort catheters, the current status of the Bard PowerPort MDL, the role of an attorney, and much more.

What is the Bard PowerPort Lawsuit and Who is Eligible to File a Claim?

The Bard PowerPort Lawsuit involves claims that certain Bard PowerPort devices, used for long-term vascular access, were defectively designed and manufactured.

Patients across the country have reported severe complications, including catheter fractures, infections, blood clots, and device migration.

These adverse events have been traced back to the materials and construction of the device, which may degrade over time and cause internal injuries.

Lawsuits allege that Bard Access Systems and its parent company, Becton, Dickinson and Company, failed to adequately warn healthcare providers and patients about the risks associated with their medical device.

Despite its widespread use in chemotherapy and long-term IV treatment, the Bard PowerPort device has now been linked to life-altering complications and emergency surgeries.

Thousands of pending Bard PowerPort Lawsuits have been consolidated in multidistrict litigation (MDL No. 3081) in the United States District Court for the District of Arizona.

Plaintiffs are seeking compensation for the physical, emotional, and financial toll these injuries have caused.

Our Bard PowerPort Lawyers are investigating these claims and helping individuals file Port Catheter Lawsuits against Bard Access Systems Inc.

Bard PowerPort Lawsuit; Bard Power Port Lawsuit; Bard PowerPort Injury Lawyers; Bard PowerPort Lawyers; Bard PowerPort Lawsuits;
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Do You Qualify for the Bard Power Port Lawsuit?

If you or a loved one have been injured by a Bard PowerPort Device, you may be eligible to file a Bard PowerPort Lawsuit and seek financial compensation.

Contact a PowerPort injury lawyer from TorHoerman Law for a free, no-obligation case consultation.

You can also use our chatbot below to receive a free, instant online case evaluation and find out if you qualify for a Bard PowerPort Lawsuit instantly.

Our law firm is committed to helping people harmed at no fault of their own seek financial compensation for what they’ve been through.

We aren’t afraid to take on large companies and manufacturers of potentially defective medical devices.

Reach out to us for more information and to find out if you qualify for legal action.

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Bard PowerPort Lawsuit; Bard Power Port Lawsuit; Bard PowerPort Injury Lawyers; Bard PowerPort Lawyers; Bard PowerPort Lawsuits;

Lawsuit Updates

April 11, 2025

The Bard PowerPort Lawsuit is ongoing. 

Law firms nationwide are continuing to receive inquiries from individuals who believe they’ve been harmed by the Bard PowerPort implantable port device.

The current lawsuit cases involve a range of reported injuries and complications, but may not include all claims against Bard PowerPort.

To help affected individuals understand whether they may qualify for legal action, we are providing the most up-to-date criteria for currently accepted injuries in the Bard PowerPort lawsuit.

As of April 2025, the following injuries are most commonly being accepted in active litigation:

  • Catheter Fractures: The catheter portion of the Bard PowerPort may crack or break, potentially releasing fragments into the vascular system.
    • These fragments can migrate, causing internal injury or requiring surgical intervention.
  • Device Migration: In some cases, the device or its components may shift from their intended position, which can result in damage to blood vessels or nearby organs.
  • Infections: The implantation or long-term use of the PowerPort may introduce bacteria or other pathogens into the body, leading to localized or systemic infections that may require hospitalization or additional treatment.
  • Thrombosis: Blood clots can develop around the catheter tip or along the length of the catheter, increasing the risk of embolism or vascular blockage.
  • Cardiac Complications: Though rare, some patients have reported that fractured catheter pieces reached the heart, leading to arrhythmias, perforations, or other serious cardiac events.

It’s important to note that the list of accepted injuries in this litigation is continually evolving as new information and reports emerge.

If you or a loved one has experienced a complication after receiving a Bard PowerPort—even if it’s not listed above—you may still qualify for legal representation.

For those experiencing complications, it is strongly recommended to consult with an attorney for a free case review.

April 11, 2025
April 1, 2025

The Bard PowerPort litigation saw a notable increase in filings from March to April 2025.

In March, there were 1,112 total new cases filed, while in April, the number of filings rose to 1,205, reflecting an increase of 93 new cases.

This rise in filings indicates continued legal action being taken by individuals who have experienced harm due to the Bard PowerPort device.

The ongoing litigation suggests that more affected individuals are coming forward to join the multidistrict litigation, seeking compensation and accountability from the manufacturer.

If you or a loved one have been injured by a Bard PowerPort Device, you may be eligible to file a Bard PowerPort Lawsuit and seek financial compensation.

Contact a PowerPort injury lawyer from TorHoerman Law for a free, no-obligation case consultation.

You can also use our chatbot below to receive a free, instant online case evaluation and find out if you qualify for a Bard PowerPort Lawsuit instantly.

April 1, 2025

Bard PowerPort Lawsuit Updates and Overview

The Bard PowerPort Lawsuit involves claims that the Bard PowerPort device, a type of implantable port used for long-term vascular access, is defectively designed and prone to serious complications.

Plaintiffs allege that flaws in the catheter material—particularly the use of Chronoflex AL with high concentrations of barium sulfate—make the device vulnerable to cracking, fracturing, and migrating inside the body.

These issues have led to severe infections, blood clots, and in some cases, life-threatening events such as sepsis, pulmonary embolism, or cardiac complications.

Bard PowerPort Lawsuits claim that Bard Access Systems and its parent company, Becton Dickinson, failed to adequately test the device or warn patients and physicians of the risks associated with its use.

Bard PowerPort Lawsuit

In August 2023, the United States Judicial Panel on Multidistrict Litigation consolidated federal cases into the Bard PowerPort multidistrict litigation (MDL 3081) in the District of Arizona, overseen by Judge David G. Campbell.

Since then, the MDL has grown steadily, with over 1,200 lawsuits pending.

The litigation is currently in the discovery process, during which both sides are gathering documents, deposing witnesses, and evaluating scientific and engineering evidence surrounding the Bard PowerPort’s design and manufacturing.

A bellwether trial plan is in place, with the first group of test cases expected to be selected and prepared throughout 2025.

These early trials will help assess how juries respond to claims of design defects, failure to warn, and negligent manufacturing.

While the outcomes of bellwether trials will not be binding for other plaintiffs, they are expected to shape the direction of potential global settlements in the Bard PowerPort MDL.

What Is the Bard PowerPort Device and Why Are Lawsuits Being Filed?

The Bard PowerPort is an implanted port catheter system manufactured by Bard Access Systems and Bard Peripheral Vascular, subsidiaries of medical device conglomerate Becton, Dickinson and Company.

It is designed to provide long-term access to a patient’s vascular system for repeated intravenous treatments such as chemotherapy, antibiotics, and parenteral nutrition.

Bard Power Port Lawsuit Settlement Amounts; Bard PowerPort Lawsuit; Bard Power Port Lawsuit; Bard PowerPort Lawsuits; Bard Power Port Device; Projected Bard PowerPort Lawsuit Settlement Amounts; Bard PowerPort Lawsuit Overview; What Is The Bard PowerPort Device

The Bard PowerPort Device consists of two parts:

  1. The Injection Port, implanted underneath the skin on an arm, or in the chest, the injection port allows easy access for injections and is made of a self-sealing material that allows multiple needle punctures.
  2. The Polyurethane Catheter is a small, flexible tube connected to the port, and is installed inside one of the large central veins that take blood to your heart.

To use the PowerPort, medical professionals need to use a special needle (the PowerLoc needle) to “access” the bloodstream.

From there, medicine and fluids can be administered through the needle and blood samples can be withdrawn.

While this medical device is intended to reduce the need for repeated needle sticks and support critical treatments, serious concerns have emerged about its safety and long-term durability.

Reports of Device Defects and Patient Harm

Thousands of patients have reported complications involving catheter failure, migration, and infection after receiving a Bard implanted port catheter.

In many cases, the polyurethane catheter—often made with a polymer blend called Chronoflex AL—has fractured or degraded over time.

Fragments of the device may travel through the blood vessels, leading to vascular damage, embolisms, and other internal injuries.

These failures have triggered emergency medical procedures and even permanent harm for affected users.

Experts argue that the material, which contains high concentrations of barium sulfate to improve imaging visibility, may weaken the structural integrity of the catheter over time.

Legal Action Against Medical Device Manufacturers

As of 2025, more than a thousand plaintiffs have filed Bard Port Catheter Lawsuits in federal court, claiming that certain Bard PowerPort devices are defectively designed and pose unreasonable risks to patient safety.

Plaintiffs also allege that Bard and other medical device manufacturers failed to adequately test the materials used and failed to warn patients and physicians about the potential for severe injury.

These claims have been consolidated into the Bard PowerPort multidistrict litigation (MDL) to streamline the pretrial proceedings and organize the growing number of lawsuits.

The MDL allows plaintiffs from across the country to file Bard PowerPort Lawsuits without duplicating discovery and to hold Bard accountable under a unified legal framework.

How Many Bard PowerPort Lawsuits Have Been Filed? Current Status of the Bard PowerPort MDL

The Bard PowerPort MDL continues to grow, with roughly 900 pending Bard PowerPort Lawsuits filed as of January 2025.

New Bard PowerPort Lawsuits are currently being filed by lawyers across the country.

If you were injured or suffered other Bard PowerPort complications, you may be eligible to file a Bard PowerPort Lawsuit and seek compensation.

Contact TorHoerman Law for a free consultation.

You can also use the chatbot on this page to find out if you qualify for a Bard PowerPort Lawsuit.

Bard PowerPort Settlement Amounts: Projections & Estimates

Bard PowerPort lawsuits are still in early stages, and no settlements have been reached.

However, attorneys estimate that potential Bard PowerPort settlement amounts could range between $10,000 and over $250,000, depending on individual damages and the direction of the litigation.

These figures are general estimations and not guaranteed, as each case is unique and outcomes can vary.​

While exact settlement figures are not yet determined, attorneys have provided estimated ranges based on the severity of injuries:

  • Tier 1 – Severe Injuries: Cases involving life-threatening complications such as cardiac punctures, pulmonary embolism, or stroke. Estimated settlements may exceed $100,000.
  • Tier 2 – Moderate Injuries: Cases with significant injuries like deep vein thrombosis, catheter infections, or hematomas. Estimated settlements range between $50,000 and $100,000.
  • Tier 3 – Mild Injuries: Cases involving less severe complications requiring minimal medical intervention. Estimated settlements range between $10,000 and $50,000.​

These estimates are based on similar previous litigations and are meant to provide a general idea of potential settlement ranges.

For a more accurate assessment of your case, it’s advisable to consult directly with a qualified attorney.​

Bard PowerPort Complications: Serious Health Risks Linked to the Bard Power Port Device

The PowerPort implantable port catheter device was designed to simplify long-term vascular access, but serious injuries have been reported due to device failure.

The most common complication involves catheter fracture, where the tubing breaks inside the patient’s body.

These fractured components can migrate through the bloodstream, a phenomenon known as catheter migration, which can cause internal damage to organs and blood vessels.

Patients have required emergency interventions when fragments lodged in or near vital organs such as the heart and lungs.

Infections originating from the PowerPort site, or along the catheter itself, have also been reported, leading to bloodstream infections and sepsis in some cases.

Another major concern is deep vein thrombosis (DVT), which occurs when blood clots form around the device or its components.

These clots can travel and result in a pulmonary embolism, stroke, or other life-threatening events.

Allegations in Bard PowerPort Lawsuits filed suggest that the device’s material composition may weaken over time, making catheter infection, fracture, and migration more likely.

Bard PowerPort Lawsuit

Serious Injuries and Complications Related to the Bard PowerPort Device include:

Complications From A Catheter Fracture

A fractured implantable vascular access device can cause significant internal damage with the catheter pieces circulating in the bloodstream.

In all cases, there is a high possibility of requiring emergency surgery to remove any fractured pieces and properly treat all affected organs.

Catheter Fracture Injuries include:

  • Cardiac Arrhythmia
  • Pulmonary embolism
  • Cardiac Punctures
  • Blood Clots
  • Hematomas
  • Lacerations to blood vessels

Complications From A Catheter Infection

An infection could potentially cause serious complication as the body could possibly have more difficulty dealing with the pathogens that reside in the catheter.

If gone untreated, catheter infection can cause a number of serious and even life-threatening injuries.

Catheter Infection Injuries:

  • Infections of the bloodstream
  • Swelling, tenderness, and soreness at the site of the Bard PowerPort implant
  • Necrosis of tissues around the Bard PowerPort implant

What Bard PowerPort Devices are Named in the Lawsuit?

Bard PowerPort devices are typically used in patients who require long-term or repeated intravenous treatments, such as chemotherapy, antibiotic therapy, or parenteral nutrition.

These implantable port catheter systems are inserted beneath the skin to access the patient’s vascular system more efficiently over extended periods.

However, certain models have been linked to severe complications, and multiple Bard PowerPort devices are specifically named in the lawsuits.

These models are alleged to contain design or material defects that may lead to catheter failure, migration, or serious injury.

Bard PowerPort Devices Named in the Lawsuit:

  • Bard PowerPort™ ClearVue Implantable Port – Commonly used in cancer patients; known for risk of catheter fracture and migration.
  • Bard PowerPort™ MRI Implantable Port – Marketed as MRI-compatible, but lawsuits claim it may be prone to cracking and failure.
  • Bard PowerPort isp M.R.I. Implantable Port – Frequently cited in complaints involving infection, thrombosis, and device degradation.
  • Bard PowerPort™ SlimPort Implantable Port – A smaller-profile device included in legal filings for similar safety concerns.
  • Bard PowerPort™ Dual-Lumen Port – Allows for multiple lines of medication but has been linked to complications from design flaws.

Each of these devices has appeared in Bard PowerPort Lawsuits due to alleged structural instability or unsafe materials that may put patients at risk.

Do You Qualify to File a Bard PowerPort Lawsuit?

Many Bard PowerPort cases have been filed by individuals who experienced serious complications after receiving the implantable port device manufactured by Bard Access Systems Inc.

If you were implanted with a Bard PowerPort and later experienced a catheter fracture, migration, or infection, you may be eligible to file a Bard Power Port Lawsuit.

These lawsuits claim that the devices were defectively designed and inadequately tested, leading to a wide range of preventable injuries.

To participate in the ongoing litigation, new plaintiffs are required to submit a short form complaint detailing their specific injuries and identifying the Bard device used.

Bard PowerPort Lawsuit

If your case qualifies, it will be reviewed alongside other Bard PowerPort cases that are part of the MDL in the District of Arizona.

Plaintiffs are alleging negligence, manufacturing defects, and a failure to warn about the risks associated with these devices.

Contact TorHoerman Law today to find out whether you meet the qualifications to join the Bard PowerPort Lawsuit.

Our law firm has decades of experience handling lawsuits for defective medical devices and holding manufacturers liable for their negligence.

Our Bard PowerPort Injury Lawyers are here to help you through the legal process, helping you through different steps of the lawsuit such as mitigation, hiring a lawyer, gathering evidence and assessing damages.

Mitigate Your Injuries

If you believe something is wrong with your implanted port device or feel pain around the port device’s location, you should see your doctor immediately to receive the necessary care.

It’s important to treat any PowerPort injury early.

Make sure to follow their orders, do everything in your power to mitigate future economic impacts related to your injury.

Hiring A Bard PowerPort Injury Lawyer

The civil litigation process requires extreme attention to detail and can be overwhelming for someone who does not possess extensive legal knowledge.

Bard PowerPort Lawsuit

An experienced Bard PowerPort injury lawyer can help you to:

  • Determine liability
  • Gather evidence
  • Assess damages
  • Build a strong case
  • Get you compensated for your injuries

Contact the attorneys at TorHoerman Law today for a free, no-obligation legal consultation to see if you qualify for a Bard PowerPort catheter injury lawsuit.

Keep in mind, the statute of limitations limits the amount of time you have to take legal action after an injury, so do not wait to take the first step by contacting an attorney.

Gathering Evidence for a Bard PowerPort Lawsuit

Gathering strong evidence is essential for building a successful case in the Bard PowerPort litigation.

Plaintiffs must show a clear connection between their injuries and the Bard Power Port implant, supported by detailed documentation.

Medical records are among the most important types of evidence, as they help demonstrate the extent of harm and necessary treatments.

Additional forms of evidence can support claims of product failure and the manufacturer’s liability.

Bard PowerPort Lawsuit

Evidence in a Bard PowerPort Lawsuit may include:

  • Medical Records – These provide proof of implantation, diagnosis, treatment, and complications linked to the Bard PowerPort.
  • Surgical Reports – Documentation of implantation and explantation procedures can help demonstrate how the device may have caused harm.
  • Imaging Results – X-rays, CT scans, or ultrasounds may show catheter fracture, migration, or related damage.
  • Device Identification Information – Details about the specific Bard PowerPort model implanted, including serial number and implant date.
  • Photos or Videos – Visual documentation of visible injuries, device fragments, or post-surgical conditions.
  • Personal Testimony – Written or recorded statements describing the pain, limitations, and emotional impact of injuries.
  • Expert Opinions – Statements from medical professionals supporting the link between the Bard device and the injury.

Thorough and well-organized evidence strengthens your claim and gives your legal team the foundation they need to pursue compensation.

Assessing Damages in a Bard PowerPort Lawsuits

In Bard PowerPort Lawsuits, damages refer to the financial, physical, and emotional losses a person suffers as a result of complications caused by the implantable port catheter device.

These damages form the basis of compensation sought in litigation and can vary significantly depending on the severity of injury and long-term impact.

Bard PowerPort Lawsuits allege that design and manufacturing flaws led to preventable harm, making injured individuals eligible to pursue both economic and non-economic damages.

A Port Catheter Injury Lawyer can help evaluate your case, calculate losses, and build a claim that reflects the full scope of your suffering.

Bard PowerPort Lawsuit

Potential Damages in a Bard PowerPort Lawsuit may include:

  • Medical Bills – Reimbursement for past, current, and future expenses related to treatment, surgeries, hospital stays, and medication.
  • Lost Wages – Compensation for income lost due to time off work or reduced earning capacity.
  • Pain and Suffering – Monetary damages for the physical pain and emotional distress resulting from the injury and ongoing complications.
  • Loss of Enjoyment of Life – Recovery for limitations placed on hobbies, relationships, or daily activities due to the injury.
  • Permanent Disability – Financial recovery for long-term impairment or disfigurement caused by the Bard PowerPort device.
  • Out-of-Pocket Expenses – Includes travel costs, home modifications, or assistive devices required after the injury.

Bard PowerPort Lawyers can help you assess and calculate losses to advocate for the full amount of compensation you deserve.

TorHoerman Law: Your Bard PowerPort Injury Lawyers

Our team of dedicated attorneys, with more than 100 years of combined litigation experience, have helped clients win more than $4 billion in verdicts and negotiated settlements for injuries suffered at no fault of their own.

If you or a loved one were injured by Bard PowerPort devices, you may be eligible to file a Bard PowerPort Lawsuit against the medical device manufacturer.

Contact TorHoerman Law for a free consultation.

You can also use the chatbot on this page to find out if you qualify for a Bard PowerPort Lawsuit instantly.

Our attorneys work on a contingency fee basis – so our clients don’t pay any legal fees unless they are awarded compensation for their injuries & other losses.

Reach out to us if you were injured by a defective device. We’re here to help you.

Frequently Asked Questions

  • What is the Bard PowerPort Lawsuit?

    Bard PowerPort Lawsuit claims are being filed against the manufacturers of the Bard PowerPort, an implantable port catheter device used for administering medications like chemotherapy.

    Bard PowerPort lawsuits allege that the device has design flaws, leading to severe complications such as infections, blood clots, and device fractures.

    Plaintiffs claim that Bard Access Systems, Inc. and its parent company (Becton Dickinson and Company) were aware of these risks but failed to adequately warn patients and healthcare providers.

    Victims are seeking compensation for medical expenses, pain and suffering, and other damages resulting from the device’s malfunctions.

    The central claim is that the manufacturers did not properly test or disclose the risks associated with the PowerPort — leading to claims of negligence and strict liability.

    These lawsuits aim to not only secure compensation for those injured but also to push for better safety warnings and accountability from medical device manufacturers.

  • Is There a Bard PowerPort Recall?

    Currently, there is not an active Bard PowerPort recall.

    In March 2020, the FDA issued a Class 2 recall for certain Bard PowerPort models, but that recall was unrelated to the core design flaws alleged in the litigation.

    The 2020 recall focused on issues with incorrect tunneler components, not the material degradation or device failures at the heart of the lawsuits.

    As of now, no recall has addressed the catheter fractures, device migration, or infections linked to Bard PowerPort complications.

    Despite the absence of a current recall, lawsuits continue to move forward due to mounting reports of serious health complications.

    Plaintiffs argue that Bard Access Systems and its parent companies should have warned patients and providers about the risks associated with the PowerPort’s long-term use.

    People who’ve suffered injuries after being implanted with a Bard PowerPort Device are encouraged to reach out to our experienced Bard PowerPort Injury Lawyers for a free consultation.

    Contact us or use the chatbot on this page to find out if you qualify to file a Bard PowerPort Lawsuit instantly.

  • What is the Average Bard PowerPort Settlement Amount?

    The Bard PowerPort Lawsuit is still in its early stages and no settlements have been reached.

    However, attorneys estimate that the average Bard PowerPort settlement may range between $10,000 to over $250,000 depending on an individual’s damages and the direction of the litigation.

    These estimates are by no means a guarantee of compensation in the Bard PowerPort Lawsuit; they are merely projections based on results in past product liability lawsuits.

    An experienced Bard PowerPort Lawyer can help determine if you qualify to file a Bard PowerPort Lawsuit and what to expect.

    Contact TorHoerman Law for a free discussion about your legal options and the Bard PowerPort Lawsuit.

  • Is There a Bard PowerPort Class Action Lawsuit?

    No, there is not a Bard PowerPort class action lawsuit—instead, the litigation is proceeding as a Bard PowerPort MDL, or multidistrict litigation.

    The Bard PowerPort Lawsuit involves more than 1,000 individual claims filed by people who suffered injuries from the Bard implanted port catheter device, which has been linked to serious health risks such as infection, catheter fracture, and blood clots.

    An MDL is different from a class action in key ways.

    In a class action, one lawsuit represents a group of people with nearly identical claims, and any settlement or verdict is shared among all members of the class.

    In contrast, a multidistrict litigation keeps each plaintiff’s case separate, allowing for individualized outcomes based on specific injuries and circumstances.

    The Bard PowerPort MDL consolidates these lawsuits for efficiency during pretrial proceedings, but each plaintiff retains control over their case.

    This structure is common in product liability litigation where injuries and outcomes vary widely.

  • How Is the Bard PowerPort Lawsuit Progressing in Court?

    The Bard PowerPort Lawsuit is advancing through a federal multidistrict litigation (MDL), with over a thousand cases centralized in the U.S. District Court for the District of Arizona.

    In a January 2024 status conference, the MDL judge issued a key ruling allowing plaintiffs to depose Bard’s sales representatives in person—a major development that could uncover internal communications about the risks linked to the Bard implanted port catheter device.

    These depositions are expected to play a pivotal role in uncovering what Bard Access Systems Inc. knew about the serious health risks associated with catheter migration, fracture, and infection.

    The judge also addressed discovery delays and compliance issues, emphasizing the importance of both sides meeting procedural obligations.

    As the litigation moves toward bellwether trials, each status conference continues to shape the trajectory of the Bard PowerPort MDL.

  • How Are Bellwether Trials Being Selected in the Bard PowerPort Lawsuit?

    Bellwether trial selection in the Bard PowerPort MDL is underway and follows a structured process managed by the court.

    In the March 2025 case management conference, Judge David G. Campbell extended the deadline for selecting six bellwether cases to April 21, 2025, after both sides narrowed an initial group of 24 lawsuits down to 15.

    These selected cases will undergo expert discovery and serve as early test trials to help assess the strength of claims involving catheter fracture, migration, and infection.

    The bellwether trials won’t set binding precedent but will influence potential global settlements.

    The selection process is a critical step in mass tort litigation and helps clarify how juries may respond to recurring allegations in the Bard PowerPort Lawsuits.

  • What Serious Injuries are Linked to the Bard Power Port Device?

    The Bard PowerPort catheter device has been linked to a number of serious, sometimes life-threatening injuries.

    Many of these complications are the result of catheter migration, material degradation, or structural failure within the device.

    Patients have reported sudden health emergencies and long-term medical issues after receiving a Bard PowerPort implant.

    These risks have become central to the litigation, as plaintiffs argue the manufacturer failed to disclose the full scope of danger.

    Below are some of the most commonly reported injuries associated with the device:

    • Catheter Migration: Movement of the catheter from its original placement, potentially causing damage to nearby organs or tissues.
    • Blood Clots: Can develop around the device or dislodged fragments, increasing the risk of blockage in critical veins or arteries.
    • Deep Vein Thrombosis (DVT): A serious condition where clots form in deep veins, usually in the legs, with risk of pulmonary embolism.
    • Vascular Damage: Fractured catheters can tear or puncture blood vessels, leading to internal bleeding or the need for emergency surgery.
    • Infections: Bacteria may colonize cracked surfaces, leading to localized or systemic infections such as sepsis.

  • What is a Catheter Fracture?

    A catheter fracture would occur when part of a catheter device breaks inside of the patient’s body.

    In some cases, the catheter can potentially break down further once in the bloodstream, which could potentially cause fragments of silicone and polyurethane to travel the circulatory system.

  • What causes a catheter fracture?

    A catheter often fractures due to the lower durability that results from constantly flexing or moving the muscles near the PowerPort.

    This issue is known as flex fatigue.

  • What is a Catheter Migration?

    Catheter Migration can be rare but is a serious complication with an implanted PowerPort.

    Due to varying reasons, a catheter may completely dislodge itself from the Powerport and migrate to other organs in the body’s circulatory system.

    This means that a dislodged catheter may travel to vital organs, such as the heart, and lodge themselves there, requiring immediate surgery and extraction.

  • What causes catheter migration?

    Two reasons for catheter migration include:

    1. Improper installation of the PowerPort port device.
    2. Manufacturing defects of device

    The manufacturer of the implanted PowerPort device (Brad Access System) may also be held liable for catheter dislodgment and subsequent migration due to manufacturing errors of the device.

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Tor Hoerman

Owner & Attorney - TorHoerman Law

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In this case, we were able to successfully recover $20 Million for our client after they suffered a Toxic Tort Injury due to chemical exposure.

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$103.8 Million
COX-2 Inhibitors Injury

In this case, we were able to successfully recover $103.8 Million for our client after they suffered a COX-2 Inhibitors Injury.

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$4 Million
Traumatic Brain Injury

In this case, we were able to successfully recover $4 Million for our client after they suffered a Traumatic Brain Injury while at daycare.

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$2.8 Million
Defective Heart Device

In this case, we were able to successfully recover $2.8 Million for our client after they suffered an injury due to a Defective Heart Device.

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