Bard PowerPort

The Bard PowerPort for Long-Term Vascular Access Has Been Reported to Cause Severe Complications & Injuries in Numerous Patients.

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Bard PowerPort Defect Litigation Attorneys at Simon Law

At Simon Law, we specialize in representing clients harmed by defective medical devices, such as the Bard PowerPort. Our experienced legal team is dedicated to advocating for individuals who have suffered due to device fractures, infections, or other severe health complications associated with the PowerPort. We help our clients secure the compensation they deserve by providing comprehensive legal support, from initial consultation through trial. Our attorneys at Simon Law understand the complexities of medical device litigation and are committed to holding manufacturers accountable for failing to ensure patient safety.

Bard PowerPort

Our Bard PowerPort Defect Litigation Results & Resources

Bard PowerPort Lawsuit Overview

The Bard PowerPort, also referred to as the “BardPort,” is a port catheter device implanted just under the skin to...

About the Bard PowerPort

The Bard PowerPort is an implantable vascular access device used for patients requiring frequent or long-term intravenous treatments, such as chemotherapy, blood transfusions, or nutritional support. This device is implanted under the skin, typically in the chest area, and connected to a catheter leading to a large vein. The unique feature of the PowerPort is its capability for power injection, allowing high-speed administration of contrast media during imaging procedures.

However, the Bard PowerPort has been linked to severe complications, including catheter fractures, device migration, infections, and blood clots. These issues can result in significant health risks, such as organ damage or life-threatening conditions. As a result, numerous lawsuits have been filed against the manufacturer, Bard Access Systems, Inc., and its parent company, Becton, Dickinson and Company (BD). The plaintiffs allege that these companies were aware of the potential dangers but failed to adequately warn patients and healthcare providers.

What are the Main Issues Associated with the Bard PowerPort?

The main issues associated with the Bard PowerPort include:

  • Catheter fracture: One of the most critical concerns is the risk of the catheter breaking inside the body. This can lead to fragments migrating to vital organs, causing severe complication such as embolism, organ damage, and the need for additional surgery to remove the gragments.
  • Device migration: The PowerPort or its components can shift from their original position. Migration can cause punctures or damage to nearby organs and tissues, resulting in significant pain and potentially life-threatening situations.
  • Infections: Patients have reported infections at the implantation site or in the bloodstream. Infections can occur due to the device itself or from bacteria introduced during the implantation process. These infections can be severe, requiring hospitalization and intensive antibiotic treatment.
  • Blood clots: The presence of the device can lead to the formation of blood clots, which can cause venous thrombosis or even pulmonary embolism if they travel to the lungs.

These issues are at the center of numerous lawsuits, with plaintiffs alleging the manufacturers were aware of these risks but did not provide adequate warnings to patients and healthcare providers.

How Can I Determine if My Complications are Related to the Bard PowerPort?

To determine if your complications are related to the Bard PowerPort, follow these steps:

  • Consult your healthcare provider: The first step is to consult your healthcare provider. They can review your medical history, symptoms, and the timeline of your complications to assess whether they may be linked to the Bard PowerPort. This may involve diagnostic tests, imaging, or reviewing any recent medical procedures.
  • Review symptoms and complications: Consider whether your symptoms match known issues associated with the Bard PowerPort, such as pain, swelling, signs of infection, difficulty with the device’s function, or unusual symptoms like chest pain or shortness of breath, which could indicate serious complications like blood clots or device migration.
  • Check medical records: Reviewing your medical records can help determine if the device’s implantation and any subsequent issues align with known complications related to the Bard PowerPort. This includes looking for documented incidents of catheter fracture, migration, or infections following the device’s placement.
  • Seek legal consultation: If you suspect a connection, consult a legal professional experienced in medical device litigation. They can help evaluate your case, review medical records, and determine if your complications may be linked to a defective Bard PowerPort. Legal experts can also advise on the next steps if you have a viable claim for compensation.

What Compensation Can I Seek Through Litigation?

Through Bard PowerPort litigation, you may seek various forms of compensation, depending on the nature and severity of your injuries. Common types of compensation you may be entitled to include:

  • Medical expenses: This includes the cost of past and future medical treatments related to complications from the Bard PowerPort. It covers hospital stays, surgeries, medications, rehabilitation, and any necessary medical devices.
  • Pain and suffering: This compensation accounts for the physical pain and emotional distress caused by injuries or complications related to the Bard PowerPort. It considers the impact on your quality of life, including any long-term or permanent effects.
  • Lost wages and loss of earning capacity: If your injuries have caused you to miss work or affected your ability to earn a living, you may be compensated for lost wages. Additionally, if your ability to work in the future is compromised, you may seek compensation for the loss of earning capacity.
  • Punitive damages: In some cases, punitive damages may be awarded to punish the manufacturer for particularly egregious behavior, such as knowingly selling a defective product without proper warnings. These are not compensatory but serve to deter a similar conduct in the future.
  • Loss of consortium: If the complications have affected your relationship with your spouse or family members, you may be entitled to compensation for loss of companionship, affection, or support.

Each case is unique, and the specific compensation available will depend on the details of your situation.

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