When you visit a hospital, you likely trust that every medical device used in your treatment has undergone rigorous testing and approval by regulatory agencies.
Unfortunately, that isn’t always the reality.
In recent years, multiple medical device manufacturers have been sued after their products caused serious harm to patients. One such company currently facing legal action is Bard PowerPort.
Bard PowerPort manufactures a range of medical devices, including implantable port catheter devices designed for long-term medication administration, such as chemotherapy.
However, some patients have experienced severe complications linked to Bard PowerPort catheters, leading to dangerous and potentially life-threatening conditions.
As a result, hundreds of affected individuals have chosen to file a Bard PowerPort lawsuit, alleging that the company was aware of these serious health risks but failed to properly inform healthcare providers and patients.
If you or a loved one has suffered complications from a Bard PowerPort product, you may still have time to take legal action. Contact an experienced Bard PowerPort lawsuit attorney for a free case review today—schedule online or call (888) 984-6195.

What is the Bard PowerPort lawsuit about?
The Bard PowerPort lawsuit alleges that the device's design flaws caused severe complications, including infections and organ damage. Victims allege that the manufacturer failed to warn about these risks. A Bard PowerPort lawsuit lawyer can help you pursue compensation for your suffering.
What Is the Bard PowerPort?
Designed to facilitate the delivery of medications or chemotherapy treatments, Bard PowerPort is a small medical device implanted beneath the skin in the chest or arm. It consists of a catheter connected to a small reservoir or "port" that healthcare professionals can access for easy medication administration.
These slim implantable port powerport devices are often used in patients with chronic illnesses or those undergoing long-term treatment to avoid frequent needle sticks and injections.
Typically, medical devices such as these pose little to no risk to patients and are intended to improve their quality of life.
Unfortunately, this is not the case with Bard PowerPort. Instead of helping patients, these devices have caused irreparable damage, leading to diminished quality of life and decreased life expectancy.
What Makes the Bard PowerPort Dangerous for Patients?
The dangers of the Bard PowerPort are linked to a design flaw in the device. Unlike other implantable ports, the Bard PowerPort is made from a polyurethane material called Chronoflex AL, which includes barium sulfate to enhance radiological studies.
While initially, this design seemed to revolutionize the process of administering medications, it has endangered patients due to:
- Risk of microfractures: The barium sulfate can dissociate from the Chronoflex AL material, causing microfractures in the device. These fractures can lead to breaks in the catheter or port, cause a host of complications, and increase the risk of infection.
- Structural weakness: The Chronoflex AL material is also more prone to kinking or cracking than other materials used in similar medical devices. This can affect the flow of medication and increase the risk of life-threatening medical complications.
- Migration: Due to the design flaw, Bard PowerPort devices have been known to migrate from their initial implant location. This can cause severe damage to surrounding tissues and organs, leading to further complications.
These alarming side effects have caused immense suffering for patients and their families. In some cases, patients have had to undergo multiple surgeries or even face permanent disabilities due to the Bard PowerPort.
There is no excuse for putting patients at risk like this; those responsible should be held accountable for their actions.
With the help of a Bard PowerPort lawyer in the Lawsuits.com network of legal professionals, those harmed by this dangerous medical device can seek justice and compensation for their suffering.
What Health Complications Does the Bard PowerPort Cause?
The many reported complications associated with Bard PowerPort catheters include:
- Infections: The device's design flaw can lead to an increased risk of infection, which can be localized at the implant site or spread throughout the body. These infections can be difficult to treat and may require additional surgeries or long-term antibiotic therapy.
- Blood clots: The Chronoflex AL material is prone to breaking down, causing fragments to travel through the bloodstream and potentially leading to dangerous blood clots. These clots can cause serious health problems, including heart attacks or strokes.
- Organ damage: When the Bard PowerPort device migrates from its initial implant location, it can cause severe damage to surrounding tissues and organs. This not only increases the risk of infection and other complications but can also lead to permanent disabilities.
- Pain and discomfort: Due to the device's design flaw, patients have reported experiencing pain, irritation, and discomfort at the implant site. This can greatly impact their quality of life and even make it difficult for them to continue necessary medical treatments.
Unfortunately, many patients have suffered extensive injuries or died as a result of complications caused by Bard PowerPort devices during their treatment.
Why Are People Filing Lawsuits Against the Bard PowerPort Manufacturer?
Complications during medical procedures are not uncommon, but the issue with Bard PowerPort catheters is that these complications are directly linked to a design flaw in the device.
As such, plaintiffs in hundreds of ongoing cases have alleged that the manufacturer, Bard Access Systems, Inc., a subsidiary of Becton, Dickinson and Company:
- Failed to warn consumers and medical providers about the risks of using Bard PowerPort, disregarding their duty to provide safe medical devices.
- Concealed knowledge of design defects and associated complications from healthcare professionals and patients.
- Negligently designed, tested, manufactured, marketed, sold, and distributed the device without properly accounting for patient safety.
- Failed to conduct adequate post-market surveillance or initiate timely recalls despite reports of serious complications.
These allegations go far beyond the average medical malpractice case and highlight the severity of the situation.
Patients put their trust in healthcare professionals and medical devices like Bard PowerPort, only to suffer severe harm. Now they can hold the responsible parties accountable and receive the compensation they deserve.
What is the Bard PowerPort Multidistrict Litigation about?
In August 2023, the U.S. Judicial Panel on Multidistrict Litigation (JPML) consolidated all Bard PowerPort lawsuits filed in federal courts throughout the country into a single multidistrict litigation (MDL No. 3081) in the U.S. District Court for the District of Arizona.
Multidistrict litigation was created to handle multiple lawsuits with similar claims more efficiently. In the case of Bard PowerPort, patients across the U.S. filed lawsuits alleging that Bard PowerPort catheters contain design defects that caused serious health complications.
Instead of handling each case separately, the courts grouped them all into an MDL. This process helps streamline the legal process, avoids conflicting rulings, and allows both sides to test their arguments in bellwether trials before potential settlements or further litigation.
In March 2025, the number of Bard PowerPort lawsuits increased significantly. Over 1,100 cases are now part of the MDL, which is overseen by Judge David G. Campbell.
The lawsuits claim that the manufacturers, Bard Access Systems, Inc., and its parent company, Becton, Dickinson and Company, did not properly warn patients and healthcare providers about the serious risks that Bard PowerPort catheters pose. The lawsuits also allege that design and manufacturing flaws make the device prone to breakage and other failures.
In recent developments, the court has been preparing for "bellwether" trials, which are test cases that help both sides understand how future cases might proceed. The selection of these cases is expected to be finalized by April 7, 2025, with trials potentially starting in late 2025 or early 2026.
The pending cases name as defendants C.R. Bard, Inc., Bard Access Systems, Inc., Bard Peripheral Vascular, Inc., and their parent company, Becton, Dickinson and Company.
If you or a loved one had a Bard Powerport catheter implanted and have experienced complications, it's important to consult with a healthcare professional and consider seeking legal advice to understand your options. You may be eligible to seek compensation for your injuries and damages.
How Can A Bard PowerPort Lawsuit Attorney Help Me?
If you or a loved one has suffered harm due to the Bard PowerPort, joining ongoing litigation with the help of an experienced attorney is the most effective way to seek justice and compensation for your suffering.
A Bard PowerPort lawsuit lawyer can:
- Evaluate your case and determine the best course of action to seek manufacturer compensation.
- Gather necessary evidence, medical records, and expert testimonies to build a strong case for compensation.
- Negotiate with insurance companies and represent you in court to ensure that you receive fair compensation for damages such as medical expenses, lost wages, pain and suffering, and more.
These valuable legal actions significantly alleviate the stress and burden of navigating complex legal procedures while dealing with health complications.
How Much Can I Receive in a Bard PowerPort Lawsuit?
There is no set standard of compensation when it comes to medical device lawsuits, as the amount awarded can vary significantly depending on various factors, such as:
- The severity of injuries
- The amount of evidence supporting your claim
- The level of negligence displayed by the manufacturer
- The impact on daily and overall quality of life
Based on these factors, you could see compensation that covers economic and non-economic damages, including:
- The cost of current and future medical treatments related to the devices complications
- Emotional distress and trauma
- Permanent disabilities and disfigurement
- Loss of consortium
- Pain and suffering
- Funeral and burial costs for any wrongful deaths
- Lost wages or loss of earning capacity due to disability or inability to work
Additionally, your total settlement could include punitive damages. These are separate from compensation for losses and punish the defendant for their egregious actions.
To understand the value of your unfortunate damages and losses, you must consult with an experienced Bard PowerPort lawyer from our network of legal professionals. They can accurately assess the details of your case and determine how much you may be entitled to.
What Should I Do if I Bard PowerPort Harmed Me?
If the Bard PowerPort harmed you:
- Seek immediate medical attention for your safety and well-being.
- Keep records of all medical treatments, procedures, and expenses related to the complications caused by Bard PowerPort.
- Contact an experienced Bard PowerPort lawsuit attorney to discuss your legal options and determine if you have a case.
- Gather any relevant evidence or information supporting your claim, such as medical records, receipts, and communication with healthcare professionals about the device.
Due to the statute of limitations for filing lawsuits for medical device injuries, you must take the steps above as soon as possible. The longer you delay seeking medical and legal assistance, the more difficult it may be to obtain fair compensation.
Bard PowerPort Lawsuit Updates and News
With over 400 lawsuits filed across the country, justices have ordered the Bard Powerpot lawsuits to be consolidated into multi-district litigation (MDL) in the US District Court for the District of Arizona. This consolidation will help streamline the legal process and allow for the efficient handling of similar cases.
The benefits of joining in on this MDL include:
- Reduced litigation costs, as information and evidence can be shared between cases.
- Increased efficiency in case management and resolution.
- Avoiding inconsistent rulings by different courts.
- The potential for higher settlement amounts due to increased bargaining power against the defendant.
This year provides a much-anticipated set of upcoming status conferences, bellwether trials, and potential settlements.
To learn more about the current status of Bard PowerPort lawsuits and any potential updates, choose an attorney who is well-informed on the latest news and developments in this ongoing litigation.
Bard PowerPort Lawsuit FAQs
1. How much does it cost to hire a Bard PowerPort attorney?
Most Bard PowerPort lawyers work on a contingency basis, which means you do not pay any legal fees unless you receive compensation. This ensures that those affected by the adverse complications of this defective medical device have access to quality legal representation regardless of their financial situation.
2. How long will it take to resolve the Bard PowerPort lawsuit?
The time it takes to resolve a Bard PowerPort lawsuit can vary depending on your case's specific details and complexities. However, with the consolidation of cases into MDL, the legal process may be expedited compared to individual lawsuits. Your attorney can provide an estimated timeline based on your unique circumstances.
3. Should I join the Bard PowerPort lawsuit if I have not experienced any complications?
Many complications associated with Bard PowerPort can take years to develop and may not be immediately apparent. If you have had a medical procedure involving this device, you should speak to a Bard PowerPort attorney to determine if joining the lawsuit is in your best interest.
4. Will I have to testify in court?
You may have to testify in court if your case goes to trial. However, most lawsuits settle outside of court and do not require testimony from the plaintiff. Your attorney will be able to guide you through the legal process and inform you of what to expect.
5. Who is eligible to join the Bard PowerPort lawsuit?
Anyone harmed by complications from the Bard PowerPort medical device may be eligible to join the lawsuit. This includes those who received a Bard PowerPort implant, as well as family members of those who have died because of the device. Speak with an attorney to understand your eligibility to join the lawsuit.
Contact a Bard PowerPort Lawsuit Lawyer Today
The devastating consequences for those whom Bard PowerPort has harmed are unacceptable. If you or a loved one has been affected by this defective medical device, don't hesitate to begin the legal process of seeking justice and compensation.
Get connected with a licensed Bard PowerPort lawyer in your state with the help of Lawsuits.com by filling out our online form or calling (888) 984-6195.