Can I File a PowerPort Catheter Lawsuit for Blood Clots?

Powerport catheter blood clot lawsuit eligibility is a growing concern for thousands of patients. The Bard PowerPort is an implantable port catheter made by Becton, Dickinson and Company (BD). Doctors place it under the skin, usually in the chest, to deliver chemotherapy drugs or draw blood. However, many patients have reported serious complications. These include dangerous blood clots, catheter fractures, and device migration. As of 2026, more than 2,400 lawsuits have been filed against BD in federal court. These cases are consolidated in What Injuries Are Linked to the Bard PowerPort?

The PowerPort catheter has been linked to several serious injuries. Blood clots, also called thrombosis, are among the most common. Clots can form in or around the port device. In some cases, these clots travel to the lungs. This can cause a pulmonary embolism, which is life-threatening. Patients have also reported strokes linked to catheter-related blood clots.

Other reported injuries include catheter fracture and migration. The polyurethane catheter can crack or break inside the body. Broken fragments may then travel through the bloodstream to the heart or lungs. Infections at the port site, including sepsis, have also been reported. The FDA MAUDE database contains hundreds of adverse event reports for this device. Powerport catheter blood clot lawsuit eligibility typically requires documented evidence of one or more of these injuries.

Powerport Catheter Blood Clot Lawsuit Eligibility Requirements

Not everyone who had a PowerPort implanted will qualify for a lawsuit. To meet powerport catheter blood clot lawsuit eligibility standards, you generally must show several things. First, you must have had a Bard PowerPort or similar Bard port catheter implanted. Second, the device must have caused a documented injury. For example, you may have developed blood clots, experienced catheter fracture, or suffered an infection. Third, the injury must have required hospitalization or significant medical treatment.

Families of patients who died from PowerPort complications may also file wrongful death claims. In most cases, medical records showing the connection between the device and the injury are essential. Your powerport catheter blood clot lawsuit eligibility depends on the strength of this medical documentation. Patients whose ports were used solely for dialysis may face additional screening requirements.

Eligibility Factor What You Need
Device Bard PowerPort or Bard-manufactured port catheter
Injury Type Blood clots, catheter fracture, migration, infection, or death
Medical Evidence Hospital records, imaging, or surgical reports documenting the injury
Timing Within your state’s statute of limitations (typically 2–3 years from discovery)

Statute of Limitations and Filing Deadlines

The statute of limitations for powerport catheter blood clot lawsuit eligibility varies by state. Typically, you have two to three years to file. However, the clock usually starts from the date you discovered the injury — not when the device was implanted. For example, California has a two-year statute of limitations from the date of discovery. As a result, patients who learned about their PowerPort injury in 2024 or later may still have time to file in 2026.

This discovery rule is important. Many patients do not immediately connect their symptoms to the device. A blood clot may develop weeks or months after implantation. If you only recently learned that your PowerPort caused your blood clot, your powerport catheter blood clot lawsuit eligibility window may still be open. However, waiting too long could cost you your right to file. Each state sets its own deadline, so checking your state’s specific rules is critical.

Current Status of the PowerPort MDL Litigation

The federal cases are consolidated under MDL No. 3081 before Judge David G. Campbell. The Judicial Panel on Multidistrict Litigation originally transferred cases in 2023. The number of pending cases has grown steadily. In February 2025, roughly 1,004 cases were pending. By mid-2025, that number reached approximately 1,606. As of early 2026, more than 2,400 lawsuits are active in the MDL.

Both sides have submitted lists of bellwether cases for trial. These test cases cover fractures, infections, and blood clots. The first bellwether trial was scheduled for April 2026. No global settlement has been announced yet. Powerport catheter blood clot lawsuit eligibility remains available while the litigation is ongoing. The FDA has not issued a formal recall of the PowerPort. However, in April 2025, the FDA issued a safety alert for Bard PowerPICC catheters — a related product — warning of material fatigue and cracking risks.

Steps to Take If You Believe You Qualify

If you think you meet powerport catheter blood clot lawsuit eligibility criteria, there are specific steps to take. First, gather your medical records. Request documentation of your PowerPort implantation, any complications, and all related treatments. Hospital discharge summaries and imaging reports are especially important.

Second, note the timeline of your symptoms. Write down when you first noticed problems and when a doctor confirmed the device caused them. This information helps establish whether you fall within your state’s filing deadline. Third, consult with a product liability attorney experienced in medical device litigation. Many attorneys offer free case evaluations for PowerPort claims. Powerport catheter blood clot lawsuit eligibility consultations typically involve reviewing your medical records and device history.

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As a result of the growing number of cases, legal resources for affected patients have expanded. Powerport catheter blood clot lawsuit eligibility is something thousands of patients are currently exploring. Acting promptly helps protect your legal rights.

Frequently Asked Questions

How do I know if my blood clot was caused by the PowerPort catheter?

Your medical records should show the location and timing of the blood clot. Typically, clots that form near the catheter site or in veins connected to the port suggest a device-related cause. A doctor can confirm whether the PowerPort contributed to your clot, which is essential for establishing powerport catheter blood clot lawsuit eligibility.

Is there a deadline to file a PowerPort blood clot lawsuit?

Yes, each state has a statute of limitations. In most cases, you have two to three years from the date you discovered the injury. However, some states allow more time under certain circumstances. Checking powerport catheter blood clot lawsuit eligibility deadlines in your state is important because missing the window means losing your right to file.

Has there been a settlement in the PowerPort lawsuit?

No global settlement has been announced as of June 2026. The litigation is still in the bellwether trial phase under MDL No. 3081. As a result, powerport catheter blood clot lawsuit eligibility is still open for new claimants. Settlement discussions may follow the outcome of early trial results.

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Content last reviewed June 2026. If you notice any outdated information, please contact us.

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