Bard PowerPort Lawsuit Updates
Court Finalizes Six Bellwether Trials in Bard PowerPort MDL, Sets Key Witness Deadline
Judge David G. Campbell has approved six bellwether cases for trial in the Bard PowerPort multidistrict litigation (MDL), marking a critical phase in the 1,500+ lawsuit consolidated proceedings. The court also mandated that parties complete interviews with key witness Kelly Christian by August 28, 2025, ensuring testimony alignment ahead of trials. These lawsuits allege the implantable port’s catheter is defectively designed, causing fractures, migrations, and life-threatening infections in patients. The bellwether outcomes will inform broader settlement negotiations. New plaintiffs impacted by device failures remain eligible to join the active litigation.
Targeted Schedule Adjustment in Bard PowerPort Bellwether Trial
The parties in the Bard PowerPort MDL have jointly requested an amendment to Case Management Order No. 33, specifically adjusting deadlines in Miller v. Bard (24-cv-00612), a Bellwether Group 1 case. The update addresses delays in testing the plaintiff’s explanted catheter, which arrived in liquid and requires drying before analysis. Expert disclosure and deposition deadlines for this case alone are extended—plaintiff’s expert disclosures now due August 25, and defendants’ by September 22. Depositions begin October 13. Importantly, dispositive and Daubert deadlines remain unchanged. This measured revision ensures evidence integrity without disrupting the broader MDL timeline.
First Bard PowerPort Trial Set to Begin: Plaintiff Claims Severe Infection and Device Defect
The first Bard PowerPort trial in the Cook MDL is approaching, centered on a Minnesota man who developed a severe infection shortly after receiving the device for chemotherapy. Implanted in August 2022, the PowerPort was removed just two weeks later due to infection, forcing the patient to undergo additional surgery and IV antibiotic treatment via a PICC line. The plaintiff alleges defective design and manufacturing, claiming the catheter's materials degraded and allowed bacteria to grow. The lawsuit also accuses Bard of failing to warn doctors and patients about these risks and of concealing infection-related dangers, despite rising adverse event reports. The trial could set key precedents for hundreds of similar cases.
Bard PowerPort MDL Expands 17.5% in June, Reaching 1,763 Cases
The Bard PowerPort MDL increased by 263 cases in June 2025, bringing total pending cases to 1,763 – a 17.5% month-over-month growth rate. This significant acceleration in filings demonstrates sustained expansion of the litigation. The surge reflects heightened plaintiff activity as awareness grows regarding alleged device complications including fracture, migration, and infection. While case volume remains below initial plaintiff counsel projections, the consistent recent growth indicates active development of claims. The MDL continues consolidating federal lawsuits alleging injuries from implantable catheter ports manufactured by Bard (now BD) and AngioDynamics as discovery progresses toward bellwether selection.
About The Bard PowerPort Lawsuit
The Bard PowerPort is a medical device used for patients needing frequent intravenous treatments. The device has been linked to serious complications in many patients. The port is designed to provide easy access to medication, fluids, and blood draws. However, many patients have reported suffering from severe injuries when the Bard PowerPort malfunctions, such as infections, breaks, or migrations.
If you or a loved one has suffered from complications related to a Bard PowerPort, you may be entitled to compensation. Participating in the Bard PowerPort lawsuit can help you seek justice and hold the manufacturers accountable.
What Companies Are Involved?
C.R. Bard, the manufacturer of the PowerPort, is being sued for failing to properly warn patients and medical professionals about the risks associated with the port device. Many lawsuits claim that Bard was aware of the potential dangers but continued to market and sell the product to the healthcare facilities and patients without adequate safety warnings.
As more cases emerge, the fight for accountability is growing stronger. If you or a loved one has suffered from Bard PowerPort complications, you may be eligible to participate with others who are seeking justice and compensation.
Who Qualifies for the Bard PowerPort Lawsuit?
To participate in a Bard PowerPort lawsuit, you’ll need to meet certain conditions, such as:
- Implant of a Bard Powerport.
- Provide medical records showing that you received the port as a part of a medical treatment.
- Have medical documentation to connect your health problems to the PowerPort.
You may also be eligible if you have suffered from the following injury(ies):
- Blood Clots
- Cardiac Arrhythmia or Symptoms similar to a heart attack
- Cardiac Punctures
- Cardiac/pericardial Tamponade
- Migration due to breakage
- Hemorrhage/Hematoma
- Leakage at the port site
- Laceration to blood vessels
- Necrosis (Dead Tissue)
- Pulmonary Embolism (PE)
- Severe and Persistent Pain around the port/catheter
- Catheter Break (Into two or more pieces)
- Fracture (Remains one piece, no separation)
- Fractured pieces became embedded in the artery/organ.
- Fracture with pieces that broke apart and passed through the heart.
- Infection with the removal of the catheter.
- Blood Clots with Immediate Removal of Port.
- Death
We encourage you to seek legal advice to determine your eligibility. Various factors impact eligibility, and all cases are unique.
How Much Compensation Can You Expect in a Bard PowerPort Lawsuit?
The settlement amount in a Bard PowerPort lawsuit can vary depending on several factors:
- The severity of your injury from the port.
- Strength of your evidence showing the port is to blame for your health-related problems.
Determining a typical settlement amount in a Bard PowerPort lawsuit can be a complicated process. At this point, Bard PowerPort lawsuits are still in the early stages, and no global settlements or jury trials have taken place. Many factors influence each case. These factors include the severity of the complications, the strength of the medical evidence, jury decisions, and the expertise of your legal team.
It's time to act now, if you or a loved one has experienced health complications due to a Bard PowerPort. Contact us today to learn more about your options and whether you may qualify to join the lawsuit. Seeking justice can not only provide you with potential financial compensation, but also hold the manufacturers accountable for the harm caused.
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