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MDL 3081 · District of Arizona · 3,500+ cases

Injured by a fractured or migrated Bard PowerPort catheter?

The Bard PowerPort implantable port catheter is alleged to fracture and migrate inside the body, causing serious injury. Cases against C.R. Bard and Becton Dickinson are consolidated as MDL 3081. We never sell your information.

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◆ the case ◆
3,500+ Bard PowerPort cases consolidated in the federal MDL (3081)
+126% one-year growth in filed cases as more injuries surface
MDL 3081 federal consolidation in the District of Arizona
Fracture & migration the core alleged device failures

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.

The evidence

The documented basis for these claims:

How this case got here

  1. 2000s onward Bard PowerPort implantable port catheters are widely used for chemotherapy and IV access.
  2. Aug 2023 The JPML consolidates federal cases into MDL 3081 before Judge David Campbell in Arizona.
  3. 2024-2025 Case counts climb sharply as more device-failure injuries are reported.
  4. May 2026 The first bellwether trial (Cook v. Becton Dickinson) returns a defense verdict; litigation continues with more trials scheduled.

Complications linked to the Bard PowerPort

The claims center on device failure and the injuries that follow.

Catheter fracture or migration

Primary

The tubing cracks or breaks and fragments travel through the bloodstream, sometimes lodging in the heart or lungs and requiring surgical retrieval.

Blood clots (thrombosis)

Primary

Device failure can trigger clots, including deep vein thrombosis or pulmonary embolism, which can be life-threatening.

Infection and cardiac/vascular injury

Secondary

Bloodstream infection (sepsis), heart rhythm problems, perforation, and vascular damage are also claimed depending on the case.

Who qualifies

You likely qualify if

  • You were implanted with a Bard PowerPort or similar Bard port catheter
  • The device fractured, migrated, or caused a serious complication (clot, infection, cardiac or vascular injury)
  • Your implant and injury appear in medical records

Worth checking if

  • You had a port catheter but are unsure of the exact brand
  • You had a complication that may be device-related but is not yet confirmed

You probably don't qualify if

  • You never had an implanted port catheter
  • You had a port with no complications

Had a Bard PowerPort that failed and hurt you?

The 60-second check above tells you if your situation fits the criteria. Free, confidential, no obligation.

Check my eligibility →

How filing a Bard PowerPort claim works

Four steps. After the first one, the attorney's team does almost everything.

  1. 1

    Take the 60-second eligibility check

    Three questions confirm the basics: the implant, the complication, and attorney status.

    About 60 seconds.
  2. 2

    Free case review by a device attorney

    An attorney from the network reviews your answers and follows up to confirm your situation fits intake criteria.

    1 to 2 business days.
  3. 3

    Records gathered under HIPAA authorization

    If accepted, the intake team collects your implant records, imaging, and treatment history.

    3 to 6 weeks.
  4. 4

    Case filed in the litigation

    Once records are complete, your case is filed. Your attorney handles it through resolution. You can withdraw before signing a representation agreement.

    Filing within 30 days of records being complete.

Why timing matters for PowerPort claims

Every state sets a filing deadline (statute of limitations). Once it passes for your situation, the right to file is gone permanently.

If you are unsure whether you are still within the window, run the check now. The attorney review is free and the deadline question is evaluated first.

About the attorneys you'd be connected with

claimscout is not a law firm. We connect you with attorneys from a vetted network of firms that handle Bard PowerPort (MDL 3081) claims.

claimscout is a referral service. We do not provide legal advice and are not a substitute for an attorney-client relationship. Sponsored attorney advertising. Past results do not guarantee future outcomes.

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note from the founder.

You do not need to be a doctor to understand this device claim. If your Bard PowerPort failed and hurt you, your job is simply to confirm the implant and the injury.

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.

See if you qualify for a PowerPort claim →