Manufacturers of long-term implanted ports, including Bard, Medtronic, and others, are under investigation for device failures that cause life-threatening complications. If your port fractured, migrated, or caused a pulmonary embolism, you may be eligible for a major settlement.
We Are Investigating All Major Defective Implanted Ports
Whether your port was for chemotherapy, dialysis, or long-term antibiotics, if it failed, we can help. Many patients do not know their brand name, and our legal team will identify it for you and determine whether it qualifies for legal action.

Defects in implanted catheter systems can cause internal breakdown, structural instability, and contamination risks that escalate into serious medical emergencies.
Over time, catheter tubing can weaken, crack, or fracture, releasing plastic fragments directly into the bloodstream.
Structural Weak Points
Design or material vulnerabilities may increase the risk of premature mechanical failure under normal medical use.
Pressure-Related Stress
Power-injection and repeated access can strain the catheter walls, accelerating breakdown and instability.

Device Migration
If the catheter shifts from its implanted position, it can irritate or damage nearby vessels and organs.
Fragment Embolization
Broken catheter pieces may travel through the bloodstream, creating dangerous internal blockages.
Biofilm Formation
Irregular or compromised surfaces may allow bacterial buildup, increasing the risk of persistent bloodstream infections.
We handle catheter injury cases on a contingency basis, meaning there are no upfront costs, no hourly fees, and no financial risk to you. Our legal team advances the costs of investigating and building the case against large medical manufacturers. You only pay if we successfully recover compensation on your behalf. If there is no recovery, you owe nothing for fees or case-related expenses.

Most patients never chose a specific port. They trusted it was safe, properly tested, and appropriate for long-term use. When that trust is misplaced, patients are left facing consequences they never agreed to assume. Lawsuits focus on whether manufacturers adequately tested these devices, disclosed known risks, and prioritized patient safety over distribution speed.
Your Catheter May Be Under Investigation
Patients nationwide are raising serious concerns about long-term implanted catheters and whether critical safety risks were fully disclosed. If complications followed your implantation, your device may be part of a broader legal review. Complete the form to see if you may qualify for compensation.
You may qualify if:
* You received an implanted port for chemotherapy or long-term treatment
* You received an implanted port for chemotherapy or long-term treatment
* You required additional medical care following implantation

Complete a secure form to see if complications from an implanted catheter may qualify for legal action. It takes minutes and costs nothing.

If your case meets the criteria, a legal professional will contact you to explain your options and whether further action makes sense.

Qualified catheter injury claims are connected with experienced attorneys who handle these cases and guide clients through every step.
We connect you with experienced attorneys who handle Bard PowerPort catheter lawsuits and medical device claims nationwide.
Submitted information is reviewed promptly so attorneys can determine potential eligibility for a Bard PowerPort catheter claim.
National Injury Counsel works with attorneys across the United States to evaluate Bard PowerPort claims under applicable state laws.
All case reviews are free. Attorneys only get paid if compensation is recovered.
There are no upfront costs. Attorneys only collect fees if compensation is recovered through a Bard PowerPort lawsuit or settlement.
Information is submitted through a secure process, and National Injury Counsel coordinates the next steps with qualified legal professionals.

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