Why this is real and why it matters now
A port catheter (like the Bard PowerPort) is implanted under the skin to deliver chemotherapy, IV medication, or nutrition without repeated needle sticks. Plaintiffs allege the PowerPort's polyurethane material can fracture, crack, or migrate, with fragments traveling through the bloodstream and causing blood clots, infections, and cardiac or vascular injury. The federal cases are consolidated as MDL 3081 before Judge David Campbell in the District of Arizona.
The alleged defect is in the material. Plaintiffs claim the PowerPort's catheter tubing, made with a polyurethane blend, is prone to cracking, fracturing, and degrading over time. When it fails, pieces can migrate through the vascular system, and the device becomes a source of blood clots, infection, and cardiac or vascular damage.
The federal cases are consolidated as MDL 3081 before Judge David Campbell in the District of Arizona. The first bellwether trial in May 2026 returned a defense verdict, but the litigation continues to grow and additional bellwether trials are scheduled, with firms still accepting new cases.
What you might receive. No global settlement has been set; values will depend on the type and severity of the complication (fracture, migration, clot, infection, surgery) and are estimated by the firm after records review.
Common questions
What is a Bard PowerPort?
An implantable port catheter placed under the skin to deliver chemotherapy, IV medications, or nutrition. The claims allege the catheter can fracture and migrate, causing serious injury.
What injuries qualify?
Catheter fracture or migration, blood clots, bloodstream infection, and cardiac or vascular injury linked to the device. A port with no complications generally does not qualify.
The first trial was a defense verdict. Is the case over?
No. The May 2026 bellwether ended in a defense verdict, but that is one representative case. The MDL continues, more bellwether trials are scheduled, and firms are still accepting new clients.
I'm not sure what brand of port I had. Can I still check?
Yes. Start the check anyway. The attorney's team can help identify the device from your implant records.
What records do I need?
Eventually, your implant and removal records, imaging, and treatment history. You do not need all of it to start; the intake team gathers most of it under HIPAA authorization.
Do I need a lawyer first, or do you connect me?
We connect you. The check routes qualified cases to a device-litigation attorney, and you can accept or decline.
What does this cost me?
Nothing. We get paid by the law firms or affiliate fees from the
court-appointed administrator. You pay zero up front and zero out of
any payout you receive.
Will lawyers spam-call me?
Only if you check the consent box. We give you the choice. If you do
not consent, your claim is captured and we route it to the administrator
directly without sharing your phone number.
Can I file directly without you?
Yes, always. If we route your claim to a law firm, you can choose
to file directly with the same firm or pick a different one. We exist
because most people throw the notice letter away. We make it not happen.
Is claimscout a law firm?
No. We are not a law firm and do not provide legal advice. We are a
platform that captures your claim, qualifies it, and routes it to the
court-appointed administrator or a law firm of your choice.