A Medical Device Meant to Heal Should Never Cause Harm.

Trial Lawyers United represents individuals nationwide who suffered severe complications from defective Bard PowerPort implantable catheter systems.

In the Relentless Pursuit of Justice | Results without Risk

Overview

The Bard PowerPort, manufactured by C.R. Bard, Inc. (a subsidiary of Becton Dickinson), is an implantable catheter system used to deliver medications directly into a patient’s bloodstream — often for chemotherapy, antibiotics, or intravenous nutrition.

While intended to simplify treatment, thousands of patients have suffered serious injuries due to fractures, migrations, and infections linked to design and material defects in the PowerPort system. Evidence shows that Bard was aware of these risks but continued to market and sell the product without adequate warnings.

At Trial Lawyers United, we represent patients who’ve suffered life-threatening injuries caused by Bard PowerPort catheters. Our attorneys are actively involved in the ongoing federal multidistrict litigation (MDL No. 3081, District of Arizona) and are committed to holding Bard accountable for placing profits before patient safety.

Who’s Liable / How Fault Works

The Bard PowerPort litigation focuses on product liability and failure-to-warn claims against C.R. Bard and its parent company Becton Dickinson. Among other things, the lawsuits generally allege:

• Design defects: Becton marketed a device with known design defects and without sufficient safety testing.
• Failure to warn: Bard failed to adequately disclose the known risks of fracture and infection to physicians and patients.

Our firm builds each case around the timeline of Bard’s corporate knowledge, internal testing, recall history and your particular experience.

Common Device Failures and Complications

Bard PowerPort systems are designed to remain in the body for long-term access. However, design defects have led to serious complications.

These complications often require emergency surgery and may result in permanent injury, organ damage, or death.

Injuries Linked to Bard PowerPort Devices

Victims of defective Bard PowerPorts have reported severe and lasting injuries, including:

• Blood clots (deep vein thrombosis or pulmonary embolism)
• Sepsis
• Endocarditis (fluid buildup in the heart)
• Myocardial infarction (heart attack)
• Arrhythmia (irregular heartbeat)
• Sudden cardiac death
• Stroke (blood clot in the brain)
• Lacerated blood cells
• Necrosis (tissue death)
• Organ or tissue perforation caused by the implant
• Bloodstream infection

Our attorneys work with medical experts to link these injuries to PowerPort device failures using surgical records, imaging studies, and pathology evidence.

Evidence and Proof

PowerPort claims rely on both medical and corporate evidence demonstrating device defect and manufacturer negligence. Our team develops cases using:

• Medical imaging and surgical reports showing catheter fracture or migration.
• FDA adverse event reports and related data indicating device failure patterns.
• Engineering and materials testing demonstrating the device’s unsafe design.
• Testimony from treating physicians and biomedical experts to connect the defect to patient injury.

We maintain comprehensive access to MDL filings and the latest science, ensuring every client’s case is positioned strategically for resolution or trial.

How We Help

Trial Lawyers United LLC represents patients across the United States in defective medical device litigation, including the Bard PowerPort MDL. Our attorneys combine medical insight, legal experience, and national reach to hold major manufacturers accountable.

Our representation includes:

• Thorough case screening and medical record review.
• Coordination with biomedical and surgical experts to establish causation.
• Filing and managing claims within the Bard PowerPort MDL.
• Pursuing settlements or trial outcomes that reflect the full scope of injury.
• Supporting clients through every step of the litigation and recovery process.

Every case is handled on a contingency fee basis — you pay nothing unless we win.

FAQ

Q: What is the Bard PowerPort MDL?

A: The Bard PowerPort lawsuits have been consolidated into MDL No. 3081 in the District of Arizona, where coordinated pretrial discovery is underway. Parallel litigation is proceeding in state court as well.

Q: How do I know if my device was a Bard PowerPort?

A: Your surgical or hospital records should list the brand and model of your implanted port. Our team can obtain and review these records for free.

Q: What injuries are linked to the Bard PowerPort?

A: The most common include catheter fracture and migration, causing infection, blood clots, heart attack, or stroke.

Q: What does it cost to hire your firm?

A: Nothing upfront. We only get paid when we win — Results without risk.