Bard PowerPort Lawsuit Updates
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.
Bard PowerPort Litigation Surpasses 1,760 Cases with Rising Filings
The Bard PowerPort multidistrict litigation (MDL) has reached 1,763 pending cases—an increase of over 100 filings since June 2025. These claims allege severe or fatal injuries caused by implantable PowerPort devices, which are catheter ports designed to facilitate medical treatments. Plaintiffs report life-threatening complications including device fracture, migration, infection, and organ perforation following implantation. Affected individuals and families who experienced injuries or fatalities linked to Bard PowerPort complications are urged to consult legal counsel promptly. Filing a claim preserves the right to seek compensation as this litigation progresses. The rising case count reflects continued recognition of alleged device risks
PowerPort Litigation Prioritizes Claims Involving Severe Device Failures and Life-Threatening Complications
Claims in the PowerPort litigation demonstrate varying legal strength, with the most substantiated cases involving Bard or AngioDynamics ports implanted within the past decade that caused serious mechanical failures. These include device fractures, leaks, or migration resulting in blood clots, infections, pulmonary embolisms, or necessitating surgical removal. The most compelling claims involve catastrophic outcomes directly attributable to the device, such as sepsis, endocarditis, internal bleeding, vascular lacerations, or organ/tissue perforation. These life-threatening complications—often requiring emergency interventions—significantly enhance the medical and legal validity of claims by demonstrating unambiguous causation and severe harm from a device intended to facilitate treatment.
Judge Orders Bard to Revise Expert Disclosures in Ongoing Litigation
Judge Campbell has ordered Bard to revise its Rule 26(a)(2)(C) expert witness summaries for 16 individuals, citing noncompliance with disclosure standards. For three key witnesses—Christian, Powers, and Schuessler—the court found Bard’s descriptions too vague, noting they speculated on potential testimony rather than outlining expected opinions. For the remaining 13 witnesses, Bard improperly relied on deposition references without providing proper summaries. The court emphasized that this approach violates the clear requirements of Rule 26. Bard must submit all corrected disclosures by July 18, ensuring compliance before scheduled depositions proceed. The ruling underscores the importance of specificity in expert witness designations.
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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