What You Need to Know About Bard PowerPort™ Injuries and Litigation

At Jinks Crow, we’re committed to protecting people who have been harmed by defective medical devices. One device currently at the center of growing litigation is the Bard PowerPort™ — a type of implantable port used to deliver medication, chemotherapy, or other treatments directly into the bloodstream.

If you or someone you love has had a PowerPort™ implanted, here’s what you need to know:

What is the Bard PowerPort™?

The Bard PowerPort™ is a small device implanted under the skin, often in the chest or arm, that provides repeated access to a patient’s veins. It’s designed for long-term use and is commonly used during chemotherapy or for patients who need regular infusions or blood draws.

The PowerPort™ system includes a catheter that runs into a blood vessel and a port under the skin where medication can be injected.

Why Are People Filing Lawsuits?

Lawsuits have been filed across the country alleging that the Bard PowerPort™ is defective and has caused serious injuries. The most concerning problem is that the catheter (the part of the device that runs into the blood vessel) can crack, fracture, or move inside the body. When this happens, it can cause life-threatening complications, including:

• Fractures leading to catheter migration or embolization

• Perforation of organs or blood vessels

• Blood clots or deep vein thrombosis

• Sepsis or bloodstream infections

• Cardiac issues, including arrhythmia or tamponade

• Internal bleeding or hemorrhage

Some patients have required emergency medical procedures or hospitalization, and in some tragic cases, these complications have been fatal.

What’s Happening with the Lawsuits?

In August 2023, lawsuits involving Bard PowerPort™ devices were consolidated into a multi-district litigation (MDL) in federal court in Arizona. This means that many similar cases are being grouped together to streamline the legal process. The litigation is still in its early stages, but more cases are being filed as awareness grows.

Who Qualifies for a Lawsuit Due to Bard PowerPort™ Injuries?

You may be eligible to pursue a claim if:

• You had a Bard PowerPort™ or other totally implantable venous access device (TIVAD) implanted, and

• You experienced serious complications, such as a cracked or migrated catheter, infections more than 90 days after implantation, blood clots, organ damage, or required hospitalization or surgery due to the device.

If you’re not sure whether your port was a Bard PowerPort™, our legal team can help you investigate.

We’re Here to Help

At Jinks Crow, we’ve built our practice on standing up for people hurt by dangerous products. If you think your PowerPort™ may have caused a serious health issue, we’d be honored to talk with you. We can review your medical records, help determine if you may qualify for a claim, and guide you through your options — all at no cost unless we recover for you.

Contact us today for a free consultation.