If you or a loved one received a Bard PowerPort and subsequently experienced serious complications, you may be among thousands of patients now questioning whether the device itself was to blame. Litigation has emerged as patients report infections, fractures, and migrations requiring emergency intervention as a result of the device. However, not every adverse outcome with a Bard PowerPort automatically qualifies for legal action—specific criteria determine whether you have a viable claim.
Issues Associated with Bard PowerPort Devices
The main issue in Bard PowerPort litigation involves Chronoflex AL, a proprietary material used in the device’s catheter. This material combines barium sulfate with polyurethane, and according to reports filed with the FDA and claims in ongoing lawsuits, the barium sulfate component may compromise the catheter’s structural integrity over time. As the material degrades, serious malfunctions can occur:
- Catheter Breakage: When the catheter weakens, fragments can break free and travel through your bloodstream, potentially reaching your heart or lungs and creating life-threatening complications.
- Device Migration: As the catheter deteriorates, it may shift from its intended position, causing serious pain. You may require additional surgeries to remove the device,
- Infection Risks: The aging material can develop pits in the surface where bacteria colonize, dramatically increasing the risk of infection and interfering with your medical treatments.
Injuries That May Qualify for a Bard PowerPort Lawsuit
To pursue a Bard PowerPort lawsuit, you will need to demonstrate that you suffered a qualifying injury directly related to device failure. Qualifying injuries often include:
- Blood clots that form when catheter fragments or the device itself interferes with normal blood flow, potentially leading to deep vein thrombosis or pulmonary embolism
- Serious infections, such as sepsis or bloodstream infections, that develop when bacteria colonize the deteriorating catheter material
- Organ perforation caused by catheter fragments migrating through blood vessels or the device shifting and puncturing surrounding tissue
- Catheter fractures, where pieces of the device break apart inside your body, requiring emergency surgical removal
What to Bring to Your Case Evaluation
If you received a Bard PowerPort and suffered from complications linked to the device, you may have grounds for legal action. The only way to know definitively whether you have a viable case is to speak with an attorney who can evaluate your situation.
When you’re ready to discuss your situation with an attorney, gather your medical records showing the implantation date, the model implanted, and any subsequent complications or treatments. Bring records of emergency room visits, surgical interventions, or hospitalizations related to device problems.
If you have imaging studies like X-rays or CT scans showing catheter fracture or migration, include those as well. Details about how these complications have affected your daily life, your work, and your overall health provide important context that helps attorneys understand the full scope of your experience.
Speak to an Attorney about Your Eligibility
If you have experienced complications from a Bard PowerPort device, you may qualify for legal action. The criteria for pursuing a lawsuit may seem complex, but you likely have a stronger claim than you realize. Estey & Bomberger, LLP can assess your case, explain your legal options, and help you move forward with confidence. Contact us at (800) 260-7197 to speak with an attorney who will evaluate your situation at no cost.