Bard Powerport Lawsuit
The Bard PowerPort lawsuit raises critical concerns about the safety of the implanted catheter device produced by Bard Access Systems. Patients have reported serious complications linked to device failure, prompting legal action against the manufacturer. If you’ve suffered health issues after receiving a Bard PowerPort, Consumers Injury Help offers a free case review to help you explore your legal options and seek potential compensation.The Bard PowerPort lawsuit raises critical concerns about the safety of the implanted catheter device produced by Bard Access Systems. Patients have reported serious complications linked to device failure, prompting legal action against the manufacturer. If you’ve suffered health issues after receiving a Bard PowerPort, Consumers Injury Help offers a free case review to help you explore your legal options and seek potential compensation.
- This is an Active Lawsuit
What Is the Bard PowerPort Lawsuit About?
The Bard PowerPort lawsuit involves claims that implantable port devices made by Bard Access Systems, Inc. (a subsidiary of Becton Dickinson) are defective and have led to serious and sometimes life-threatening complications.
These ports are designed to deliver medications (like chemotherapy) into the bloodstream through a catheter implanted under the skin. However, lawsuits allege the devices were:
Prone to fracture or migrate
Made with defective materials (such as polyurethane mixed with barium sulfate) that degrade over time
Linked to blood clots, deep vein thrombosis (DVT), pulmonary embolism, and catheter-related infections
Who Can File a Bard PowerPort Lawsuit?
You may qualify to file a lawsuit if:
You received a Bard PowerPort device
You suffered complications, such as:
Catheter fracture
Migration of the port or catheter
Infection or sepsis
Blood clots
Heart or lung damage
You had to undergo corrective surgery, or the device caused long-term health problems
Medical documentation (records of the implantation and resulting complications) is essential for eligibility.
Side Effects and Complications Reported
The most common injuries tied to PowerPort failure include:
Deep vein thrombosis (DVT)
Pulmonary embolism (PE)
Catheter fracture or embolization (where pieces break off and enter the bloodstream)
Severe infection at the implant site
Internal bleeding or organ damage
Persistent pain and swelling
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Legal Status: Where Do the Lawsuits Stand?
Multidistrict Litigation (MDL): Bard PowerPort lawsuits have been consolidated into an MDL in federal court (District of Arizona) to coordinate pretrial proceedings and streamline the process.
Discovery phase is underway, where both sides gather evidence.
Bellwether trials (test cases) are expected to help shape future settlements.
Expected Settlement Amounts
No official settlements have been announced yet, but projected compensation ranges (based on other medical device litigations) could be:
$50,000 to over $250,000+ depending on:
The severity of injury
Medical costs (including surgeries and hospitalizations)
Long-term impact on health
Lost income or diminished quality of life
Each case is evaluated individually.
How Long Will the Lawsuit Take?
Medical device MDLs like this one typically take 2–5 years to reach resolution.
If bellwether trials begin in late 2025 or early 2026, settlements may follow if the results favor plaintiffs.
How to File a Bard PowerPort Lawsuit
Collect Your Records: You’ll need surgical and hospital documentation showing the PowerPort was implanted and caused complications.
Confirm Device Type: Ensure it was a Bard PowerPort, especially one named in the recall or litigation.
Contact an Attorney: Preferably one experienced in medical device or product liability law.
Join the MDL or File Individually: Your lawyer will determine the best path—whether as part of the MDL or an individual case.
Need Legal Help?
You can:
Contact a product liability lawyer directly
Use services like Legal Claim Assistant to connect with vetted Bard PowerPort attorneys
Get a free case review to assess eligibility
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