Judge Campbell has issued a new Case Management Order outlining critical deadlines for the ongoing litigation. Defendants must submit expert reports by May 23, 2025, with plaintiffs’ rebuttal reports due by June 20, 2025. All depositions must be completed by August 22, 2025, and motions to exclude expert testimony are due in September 2025. Additionally, both parties are required to meet and confer by April 21, 2025, to discuss the selection of bellwether plaintiffs. These deadlines ensure structured progress in the case.
The Bard Implanted Port Catheter litigation advances with the fifteenth case management conference set for Thursday. Attorneys must submit a memorandum outlining key milestones, including discovery, expert reports, and motions. Discovery disputes persist, with delays in document production and interrogatory responses. Plaintiffs’ attorneys can now attend Bard sales representative depositions, potentially revealing internal knowledge of product risks. The court ordered Bard to produce missing complaint files in eighteen cases. Bard also seeks to recover legal fees from plaintiffs for delayed profile forms, a request under court review. Bellwether trials remain a key focus as litigation progresses.
The Bard Implanted Port Catheter MDL continues to advance. The Fourteenth Case Management Conference was held on February 20, 2025, with the next scheduled for March 20. A joint memorandum outlining key litigation milestones is due by March 18. The court addressed discovery delays and ordered Bard to produce the required complaint files. The plaintiffs’ counsel secured the right to attend Bard sales representative depositions in person. Some plaintiffs face dismissal for failing to submit required forms. Bard is also seeking to recover legal fees for delayed filings, with the court allowing further briefing before making a decision.
The FDA has issued a safety alert regarding a critical defect in Bard Peripheral Vascular’s Rotarex Atherectomy System, used to remove blood clots. According to the February 6 warning, the catheter’s rotating tip may fracture due to wear, friction, or high stress, posing a risk of severe injury or death. FDA reports cite 115 incidents requiring medical intervention, including 30 serious injuries and four fatalities. The Rotarex system’s rotating helix tip is designed to clear arterial blockages, but its structural failure raises significant safety concerns for healthcare providers and patients alike.
Catheter System AlertThe 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.
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.
To participate in a Bard PowerPort lawsuit, you’ll need to meet certain conditions, such as:
You may also be eligible if you have suffered from the following injury(ies):
We encourage you to seek legal advice to determine your eligibility. Various factors impact eligibility, and all cases are unique.
The settlement amount in a Bard PowerPort lawsuit can vary depending on several factors:
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.
This is an advertisement. OnlyClassActions is not a law firm or referral service, and we do not provide legal advice. OnlyClassActions provides a free service for individuals seeking legal representation, and we do not charge you to be connected with an attorney. We do not recommend or endorse any attorneys that pay to participate. OnlyClassActions utilizes a pool of attorneys in each jurisdiction, and attorneys are selected through a round-robin process without our evaluating your legal situation when selecting which attorney will receive your information. OnlyClassActions makes no representation about the quality of legal services or the qualifications of any attorney participating in our pool. Information you submit will be shared with third-party attorney(s). An attorney-client relationship is not formed when you submit information through the form. Hiring a lawyer is a critical decision and should not be predicated solely on comments, advertisements, or other content found on any website. You are under no obligation to retain a lawyer who contacts you through this service.
Join our newsletter to stay up to date on cases and settlements.
Add Comment