Bard Powerport Lawsuit

Bard Powerport Lawsuit

We Provide Legal Help for Patients Injured by Defective Implantable Port Devices

If you or a loved one received a Bard Powerport to make chemotherapy or other intravenous treatments easier, you likely trusted that it would be safe and reliable. Unfortunately, injured patients now allege that defects in these devices can cause serious and sometimes life-threatening complications. Most Bard Powerport lawsuits involve claims from patients whose devices fractured, leaked, or caused dangerous infections, leading to additional surgeries, permanent injuries, or worse.

These devices are small, implantable ports surgically implanted under the skin, often in the chest, with a catheter that connects directly to a major vein. This design allows patients to receive medications, fluids, or nutrition without repeated needle sticks into smaller veins. 

They were meant to be a long-term solution for people facing cancer treatment, chronic illness, or other conditions requiring frequent IV access. But for some patients, these powerports created more problems than they solved.

If your Bard Powerport failed, you may be entitled to compensation for your medical bills, lost income, and pain and suffering. The team at LawsuitUpdates.com is actively pursuing these claims and can explain your legal options during a free consultation.

Key Takeaways

• The Bard Powerport lawsuit involves claims that the device can fracture, migrate, or cause infections
  
• Complications may include device breakage, blood clots, severe infections, and organ damage
  
• Many patients have required emergency surgery to remove broken or infected components
  
• Defective design and material choices are central to the lawsuits against Bard
  
• Injured patients should seek legal advice as soon as possible to avoid missing important deadlines
  

Call 888-322-3010 or fill out our secure online form to see if you qualify for the Bard Powerport lawsuit.

What Is a Bard Powerport Lawsuit?

Across the nation, injured patients have been filing individual claims related to the problems they suffered after receiving a Powerport device. Now, many of those claims have been combined into a federal Bard Powerport multidistrict litigation against C.R. Bard, Inc., the manufacturer of the Powerport and related implantable port devices. 

Bard lawsuits allege that defects in the Powerport’s design and materials make it prone to fracturing or degrading while inside the body. When this happens, pieces of the device, sometimes small shards of polyurethane or catheter tubing, can break off and travel through the bloodstream. This can cause vascular damage, blood clots, heart or lung complications, and even death.

Plaintiffs claim that Bard used materials that were too rigid or prone to wearing down, increasing the risk of cracks and breakage. They also allege that Bard failed to provide adequate warnings about these dangers to patients and healthcare providers.

What Specific Medical Complications Are Linked to Defective Bard Powerports?

Patients filing lawsuits report a range of complications linked to Powerport failures, including:

• Device fracture and migration – Pieces of the catheter or port can break off and travel to the heart, lungs, or other organs
  
• Severe infections – Bacteria can enter the bloodstream through damaged or leaking ports, causing sepsis or other dangerous conditions
  
• Blood clots – Broken or malfunctioning devices can disrupt blood flow and trigger clot formation
  
• Organ and tissue damage – Migrated fragments can puncture or damage internal organs and blood vessels
  
• Need for additional surgeries – Removal of broken devices often requires urgent and invasive procedures
  

These risks are especially troubling for patients already weakened by chemotherapy, chronic illness, or other serious conditions. For some, the additional surgeries and recovery time caused by a defective Powerport have significantly delayed their primary medical treatment.

Bard Powerport Lawsuit Updates

December 1, 2025 - Case Count Grows as Trial Nears

The Bard PowerPort lawsuits are heating up. With the first bellwether trial just a few months away, the number of people joining the litigation continues to rise, and new court filings show both sides are gearing up for a major legal showdown.

If you’re following this lawsuit because you or a loved one had complications from a Bard port implant, here’s what you need to know this month.

Case Count Passes 2,000 with Record Growth in Past Months

October and November 2025 were the busiest months yet for the Bard PowerPort litigation. A total of 155 new lawsuits were filed in the MDL, bringing the total number of active cases to more than 2,000 for the first time.

That means more patients are bringing claims that Bard’s implantable port devices caused serious injuries, like:

• Catheter fracture
  
• Infection
  
• Blood clots (thrombosis)
  
• Device migration or failure

New Plaintiffs Come Forward from Florida and Indiana

Two recent lawsuits help show the variety of patients involved in this case and the serious complications they’ve experienced.

Florida (formerly from Utah) Plaintiff

• Implanted with two PowerPort devices in 2008 and 2009
  
• Later developed thrombosis and catheter fractures
  
• Lawsuit includes claims of design defects, failure to warn, fraud, and breach of warranty
  
• She’s seeking compensatory and punitive damages from Bard
  

Indiana Plaintiff

• Received a Port SL Power 8 FR device in 2018
  
• Developed blood clots
  
• Lawsuit accuses Bard of negligence and product defects
  
• Seeking compensatory and punitive damages
  

These are just two of the many people now suing Bard and its parent company, Becton, Dickinson, for complications that required additional medical treatment or left them with permanent injuries.

Trial Prep Underway: Motions Filed Related to March 2026 Trial

The first Bard PowerPort trial is set for March 2026, and both legal teams are making key moves:

• Bard’s attorneys filed a motion for summary judgment, asking the court to throw out the case before trial.
  
• Both sides also filed motions to exclude expert testimony, challenging the other side’s medical and technical witnesses.
  

These filings are a normal part of mass tort lawsuits, but they signal that the courtroom phase is approaching—and the pressure is intensifying.

Stay Informed About the Bard PowerPort Lawsuit

If you’ve experienced complications from a Bard PowerPort—whether it fractured, became infected, or had to be removed—you’re not alone. This lawsuit is growing every month, and the first trial outcomes could shape what happens next, including possible settlements.

LawsuitUpdates.com will continue covering the latest filings, trial news, and what it means for patients seeking justice. Stay tuned for more updates as the March 2026 trial approaches.

November 1, 2025 - A Quick Summary of the Bard Litigation Through November 2025

If you or someone you love was hurt by a Bard PowerPort implant, you may be eligible to join this lawsuit and positively impact your future. Thousands of people across the U.S. have reported serious injuries caused by fractured or infected PowerPorts, and the legal fight is now moving toward its first jury trials.

What Is the Bard PowerPort Lawsuit About?

Bard PowerPort devices are small implantable ports placed under the skin to help doctors access a patient’s bloodstream for treatments like chemotherapy and nutrition. Unfortunately, many patients have experienced serious complications after implantation, with some having trouble months or even years later.

Some of the most reported issues include:

• Fractured or broken catheters
  
• Infections at or near the implant site
  
• Blood clots (thrombosis)
  
• Device migration inside the body
  

Injured patients say Bard and its parent company, Becton Dickinson, failed to properly test or warn about these risks. As a result, many people have required additional surgeries, long-term antibiotics, or even hospitalization.

How the Litigation Began

The first Bard PowerPort lawsuits were filed in 2022, as more patients began linking their injuries to this commonly used device. Due to the growing number of similar cases across the country, a federal multidistrict litigation (MDL) was created in February 2023 in the District of Arizona under Judge David G. Campbell.

The MDL allows courts to coordinate pretrial proceedings and streamline evidence gathering for these cases. It also means that early test trials—called bellwether trials—can help shape future settlements.

Where the Lawsuits Stand Now

As of October 2025, there were 1,973 active Bard PowerPort lawsuits in the MDL. That number has more than doubled since 2024, and hundreds more are expected to join.

Six bellwether trials are scheduled throughout 2026, beginning with:

• Plaintiff: Robert Cook – March 2, 2026
  
• Plaintiff: Wanda Miller – April 27, 2026
  
• Four more trials are scheduled through December 2026
  

These trials are critical. They will be the first real test of the evidence and may determine whether Bard offers a global settlement or continues fighting in court.

What’s New This Month?

New South Carolina Case

A man from Great Falls, SC, filed a new lawsuit after experiencing infection and thrombosis from multiple PowerPort implants between 2020 and 2022. His complaint claims the manufacturer produced a product with design defects and failed to warn of potential dangers. These are the same types of allegations made by hundreds of other injured patients.

FDA Receives More Injury Reports

Recent reports to the FDA describe new cases of:

• Blood clots (thrombosis) appearing more than a year after implant
  
• Sepsis and port migration, with one port pushing through a patient’s skin
  

These injuries sometimes go undetected for months or years, making early diagnosis and legal action more difficult, but not impossible.

Capsule Formation May Delay Diagnosis

A new concern has emerged. Many PowerPorts become surrounded by scar tissue created by the patient’s body. This is a process called capsule formation, which can:

• Hide fractures or leaks on medical imaging
  
• Delay symptoms or mislead doctors
  
• Complicate device removal unless special care is taken
  

If your port is being removed, doctors should photograph and preserve the tissue and catheter, as this could be useful evidence in your case.

Need Help Understanding Your Legal Options?

If you suffered complications after receiving a Bard PowerPort, you may have the right to bring a lawsuit against the device maker. Thousands of patients are stepping forward to hold the manufacturers accountable. The Lawsuit Updates team is here to help you understand your legal options and stay informed as this litigation moves forward.

Reach out today for more information or to see if you qualify to file a claim. We’ll answer all your questions during a free consultation.

Do I Qualify for the Bard Powerport Lawsuit?

You may be eligible to file a Bard Powerport lawsuit if:

• You had a Bard Powerport or similar Bard implantable port placed for chemotherapy, medication delivery, or other treatments
  
• Your device fractured, migrated, became infected, or otherwise malfunctioned
  
• You required additional medical care, hospitalization, or surgery due to device failure
  
• You suffered lasting complications, organ damage, or loss of treatment access as a result
  

Medical documentation confirming your device type, the date of implantation, and the nature of your injury will help our attorneys determine if you have a valid claim. Even if you are unsure whether your port was a Bard model, our team can often confirm this by reviewing your surgical and hospital records.

What Compensation May Be Available in a Bard Powerport Lawsuit?

If your Bard Powerport failed and caused injury, you may be entitled to financial compensation. The lawsuits against Bard seek to hold the company accountable for manufacturing and selling a defective medical device and for not providing adequate warnings about the risks.

Potential compensation may include:

• Medical expenses – Costs for hospitalization, emergency surgery, follow-up procedures, diagnostic tests, and long-term care
  
• Lost wages – Income lost while recovering, plus potential loss of future earning ability
  
• Pain and suffering – For the physical pain and emotional distress caused by complications and additional surgeries
  
• Loss of quality of life – For the long-term health effects and reduced ability to enjoy normal activities
  
• Wrongful death damages – For families who lost a loved one due to a defective Bard Powerport
  
• Punitive damages – In certain cases, to penalize the manufacturer for reckless or intentional conduct
  

Every case is unique. The value of your claim will depend on the severity of your injuries, the medical treatment required, and the evidence linking your complications to the Bard Powerport device. We can discuss your unique situation during a free case consultation.

How Long Do You Have to File a Bard Powerport Lawsuit?

Every state has a statute of limitations for product liability and medical device claims. These deadlines usually range from one to three years from the date of your injury, but in some cases, the clock starts when you first learned or should have learned that your device may have been defective.

If you delay, you risk losing your right to file a claim. This is especially important now, as Bard Powerport cases are being filed in growing numbers and have been consolidated into multidistrict litigation (MDL). Filing early can ensure your claim is preserved if a global settlement or structured resolution is reached.

How Much Does It Cost to Hire a Bard Powerport Lawyer?

When you are facing serious medical treatment and complications, as well as related bills, the last thing you should worry about is how to afford quality legal assistance. The attorneys at LawsuitUpdates.com handle Bard Powerport cases on a contingency fee basis, meaning:

• You won’t pay any upfront fees
  
• Your consultation is completely free
  
• You pay nothing unless your attorney recovers compensation for you
  

This approach allows all injured patients, regardless of income or financial status, to seek justice without adding financial strain during recovery and healing.

How Our Lawyers Can Help With Your Bard Powerport Case

A defective medical device claim is complex and often involves challenging a large medical manufacturer with significant legal resources. Our skilled and tenacious attorneys can help you by:

• Reviewing your medical history and surgical records to confirm the device type and model
  
• Collecting evidence of device failure, including medical imaging, operative reports, and pathology findings
  
• Working with medical experts to explain how the Powerport’s design or materials caused your injuries
  
• Meeting all legal deadlines and filing your claim correctly
  
• Negotiating aggressively for a fair settlement or presenting your case in court if needed
  

Our team will also manage all communication with the device manufacturer and their legal team, so you can focus on your health and your primary medical treatment.

Contact Our Trusted Bard Powerport Legal Team to Learn More

The Bard Powerport was intended to make life easier for patients facing already difficult medical challenges. Instead, for many, it has caused serious injury, delaying critical treatments, and creating new medical emergencies.

If you or someone you love was injured by a defective Bard Powerport, you may have a limited time to act. The LawsuitUpdates.com legal team is actively pursuing these cases and will review your claim for free, explain your options, and fight for the compensation you deserve.

Call 888-322-3010 or complete our confidential form today. Do not wait until it’s too late to be part of potential settlements or legal resolutions. The sooner you get started, the stronger your case can be.

Bard Powerport Lawsuit Frequently Asked Questions