Bard PowerPort Lawsuit

The Bard PowerPort is an implantable vascular access device designed for patients requiring frequent or long-term intravenous therapy. It includes two main components: an injection port placed beneath the skin and a polyurethane catheter that connects the port to a central vein. While intended to provide safe and reliable access to the bloodstream, allegations suggest that the Bard PowerPort is prone to defects that can lead to severe complications.

The device is marketed as durable and capable of withstanding high injection pressures. However, patients have reported issues such as catheter fractures, device migration, and infections, raising concerns about its safety.

Potential Complications Linked to Bard PowerPort Devices

Defective medical devices can have life-altering consequences. Injuries linked to Bard PowerPort devices include:

• Catheter fractures: Broken pieces can migrate through the bloodstream, causing internal damage.
• Infections: Device cracks may allow bacteria to enter the bloodstream, leading to life-threatening sepsis or necrosis.
• Blood clots: Deep vein thrombosis (DVT) and pulmonary embolisms have been reported.
• Organ and tissue damage: Cases of punctured veins, hemorrhage, and pericardial tamponade have been linked to device failure.
• Other injuries: Cardiac arrhythmia, collapsed lungs, and arterial punctures have also been associated with the device.

If you experience any symptoms such as pain, swelling, or difficulty breathing after the implantation of a Bard PowerPort, seek medical attention immediately.

Why Are Patients Filing Bard PowerPort Lawsuits?

Lawsuits allege that Bard and its parent company, Becton Dickinson, failed to adequately warn patients and healthcare providers of the risks associated with the PowerPort device. Plaintiffs argue that the manufacturer knew or should have known about the potential for device failure but failed to take appropriate action, such as issuing recalls or improving the product’s design.

Key claims in these lawsuits include:

• Design defects: The materials used, particularly the polyurethane mixed with barium sulfate, may make the catheter prone to fractures.
• Failure to warn: Lack of clear communication about risks such as infection, migration, and device breakdown.
• Negligence: Allegations that Bard did not adequately address adverse event reports or implement safety improvements.

Who Qualifies to File a Bard PowerPort Lawsuit?

You may be eligible to file a Bard PowerPort lawsuit if:

1. You had a Bard PowerPort device implanted.
2. You suffered complications or injuries related to the device.
3. You incurred damages such as medical expenses, lost wages, or pain and suffering due to device failure.

Our legal team can assess your case, review medical records, and determine your eligibility for compensation.

Compensation for Bard PowerPort Claims

If successful, a Bard PowerPort lawsuit could provide financial relief for:

• Medical expenses (past and future)
• Lost income or diminished earning capacity
• Pain and suffering
• Emotional distress
• Disability-related costs
• Other compensatory or punitive damages

Our attorneys will work diligently to ensure that you receive fair compensation for the harm you’ve endured.