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Active Lawsuit

Bard PowerPort Lawsuit

Had a Bard PowerPort implanted and experienced complications? You may be eligible for compensation. Get a free case review.

Settlement

In Settlements

100K+

Cases Filed/Pending

Active

Lawsuit Status

$0

Upfront Cost

Key Takeaways

Linked Injuries

Port malfunction, thrombosis, infection, vascular injury, extravasation of chemotherapy

Product

Bard PowerPort and similar implantable ports

Companies

Bard (C.R. Bard), Becton Dickinson

Status

Litigation ongoing - Settlement discussions active

About Bard PowerPort Lawsuit

Bard PowerPort devices are implantable infusion ports used primarily for chemotherapy delivery and IV access in cancer patients. These devices allow easier administration of medications while allowing patients to maintain more normal lifestyles. However, certain PowerPort models have experienced malfunction, including septal leakage, port fracture, and valve dysfunction, resulting in therapy delays and serious complications.

Cancer patients relying on these ports for critical treatment depend on them functioning properly. Malfunction can delay essential chemotherapy, leading to disease progression. Additionally, port failure can cause blood clots, infections, and vascular damage. Bard failed to adequately warn about known failure modes and risks of serious complications.

If you had a Bard PowerPort implanted and experienced malfunction, infection, thrombosis, or required surgical removal due to complications, you may have a significant claim against Bard (now owned by Becton Dickinson) for design defect and failure to warn.

Health Risks & Effects

Exposure to this product has been linked to serious health conditions and injuries. Research and case settlements have documented the following health risks:

Port malfunction and blockage
Deep vein thrombosis (blood clots)
Infection and bacteremia
Vascular injury and vessel damage
Extravasation of chemotherapy into surrounding tissue
Sepsis and systemic infection

Do I Qualify for This Lawsuit?

You may be eligible to file a claim if you meet the following criteria. Each case is unique, and a qualified attorney can provide a definitive assessment during a free case review.

PowerPort Implantation

You had a Bard PowerPort or compatible implantable port implanted for chemotherapy or IV access.

Port Malfunction

You experienced port malfunction, malposition, infection, thrombosis, or complications requiring intervention.

Medical Documentation

You have medical records documenting the port implantation and subsequent complications or revision surgeries.

Causation

Your complications were caused by port malfunction, not underlying disease or other medical factors.

Important: Family members who lost a loved one may also be eligible to file a wrongful death claim. A free case review can help determine your specific options and eligibility.

Settlements & Verdicts

Recent settlements and verdicts demonstrate the significant compensation available to qualified claimants:

2010s-2020s

PowerPort Malfunction Reports

FDA receives complaints about Bard PowerPort device failures and malfunctions.

2020-2023

Litigation Initiation

Lawsuits filed against Bard for PowerPort complications and failures.

2023-Present

Settlement Discussions

Ongoing litigation with Becton Dickinson (Bard's parent company); settlement terms being negotiated.

Settlement amounts vary based on individual circumstances, medical severity, and liability factors. Consult with a qualified attorney for personalized settlement estimates.

Lawsuit Timeline

The litigation timeline shows how this lawsuit has developed from initial complaints through current settlement discussions:

1990s-2000s

Bard PowerPort devices widely adopted for chemotherapy delivery

2000-2020

Patient complaints about port malfunction accumulate in FDA database

2015-2020

Litigation begins; multiple patients file individual claims

2020-2023

Class action lawsuits filed against Bard

2023-2024

Discovery phase; expert witness development

2024-Present

Settlement negotiations ongoing; potential MDL consolidation

How to File a Claim

Filing a claim is a straightforward process designed to minimize hassle while maximizing your recovery potential:

1

Get a Case Review

Contact LegalCove and answer brief questions about your exposure and medical condition. Your information remains completely confidential.

2

Speak with an Attorney

If you qualify, a legal advocate will contact you to discuss your situation and explain your options.

3

Get Matched

We connect you with an experienced attorney who specializes in this litigation — at no upfront cost.

Frequently Asked Questions

No, many PowerPorts function without problems. However, certain models and manufacturing runs have documented higher malfunction rates.
Causes include septal leakage, internal valve dysfunction, port fracture, and positional issues. Some failures result from manufacturing defects.
Yes, malfunctioning ports can be surgically replaced. However, replacement carries surgical risks and therapy delays.
Port malfunction causing chemotherapy delays can allow cancer progression. This may support both your medical damages claim and your legal claim.