Bard PowerPort Lawsuit | 2025 Latest Updates

Bard PowerPort Lawsuit Overview

Bard PowerPort lawsuits allege that the implantable port devices cause serious complications due to defective design.

The primary allegations against Bard Access Systems Inc. claim the company failed to warn patients and medical professionals about the risk of catheter fractures, bloodstream infections, and dangerous blood clots.

These lawsuits assert Bard PowerPort devices are unable to withstand higher injection pressure, leading to broken silicone pieces traveling through patients’ vascular systems and causing life-threatening injuries.

Latest Bard PowerPort Lawsuit Updates

• February 2023 – A Missouri woman filed a product liability lawsuit against Becton Dickinson and its C.R. Bard subsidiaries alleging that the Bard PowerPort ClearVue Implantable Port was defective and unreasonably dangerous, causing her to develop deep vein thrombosis (DVT) in her neck [1].
• February 2023 – A lawsuit was filed in the U.S. District Court for the District of New Jersey alleging that a defective polymer design used with the Bard implanted port increases the risk of catheter bloodstream infections, dangerous blood clots, and punctured blood vessels [2].

FDA Reports and Statistics

The FDA has received numerous adverse event reports through the MAUDE database regarding complications with Bard PowerPort devices. These reports detail instances of:

• Catheter migration and fracture
• Bloodstream infections
• Thromboembolism (blood clots)
• Device failure requiring surgical removal

While specific numbers are not provided in the original article, these adverse events have prompted multiple lawsuits against the manufacturer.

Bard PowerPort Injuries & Side Effects

Patients implanted with Bard PowerPort devices have reported a range of serious complications requiring medical intervention and hospitalization.

• Catheter Fractures: Broken pieces of the catheter migrating through the vascular system
• Bloodstream Infections: Serious infections requiring hospitalization
• Deep Vein Thrombosis: Dangerous blood clots in major veins
• Device Failure: Malfunction of the port requiring surgical removal
• Hematoma: Collection of blood outside blood vessels
• Vascular Damage: Punctured or damaged blood vessels

Do You Qualify for a Bard PowerPort Lawsuit?

You may qualify for a Bard PowerPort lawsuit if:

• You were implanted with a Bard PowerPort device
• You experienced serious complications such as catheter fracture, infection, blood clots, or device failure
• Your injuries required medical treatment or hospitalization
• You can provide medical documentation linking your injuries to the Bard PowerPort device

Evidence Required for a Bard PowerPort Lawsuit

To strengthen your case, you will need to provide:

• Medical records confirming the implantation of a Bard PowerPort device
• Documentation of complications or injuries you experienced
• Medical records showing treatment for these complications
• Evidence that your healthcare provider linked your injuries to the Bard PowerPort device

Damages You Can Recover

By filing a Bard PowerPort lawsuit, you may be entitled to compensation for:

• Medical expenses for treatment of complications
• Lost wages due to inability to work
• Pain and suffering
• Punitive damages against the manufacturer

Statute of Limitations for Bard PowerPort Lawsuits

The time you have to file a Bard PowerPort lawsuit varies by state.

Generally, the statute of limitations begins from the date you discovered or reasonably should have discovered that your injuries were caused by the Bard PowerPort device.

It is crucial to consult with an experienced attorney as soon as possible to ensure your claim is filed within the applicable timeframe.

Related Articles:

• Catheter Injury Lawsuit
• TIVAD Lawsuit

Frequently Asked Questions

1. What is a Bard PowerPort device and why is it used?

A Bard PowerPort is an implantable medical device used to provide easy access for delivering medications, chemotherapy, nutrients, and other treatments directly into a patient’s bloodstream. The device consists of a port with a silicone septum and a catheter that is inserted into the vascular system, typically placed under the skin of the chest or arm.

2. What specific injuries are associated with Bard PowerPort devices?

Reported injuries include catheter fractures, bloodstream infections, deep vein thrombosis (blood clots), device failure requiring surgical removal, hematoma formation, and damage to blood vessels. These complications often require hospitalization and additional surgical procedures to address.

3. How do I know if my catheter port is a Bard PowerPort?

Your medical records should indicate the specific type of port that was implanted. You can request these records from the hospital or healthcare provider who performed the implantation procedure. The operative report typically contains details about the brand and model of the implanted device.

4. How long do I have to file a Bard PowerPort lawsuit?

The statute of limitations varies by state but typically ranges from 1-3 years from the date you discovered your injury was related to the device. It’s important to consult with an attorney as soon as possible to ensure your claim is filed within the applicable timeframe.

5. What compensation can I receive from a Bard PowerPort lawsuit?

Potential compensation includes recovery for medical expenses, lost wages, pain and suffering, and in some cases, punitive damages. The exact amount depends on the severity of your injuries, impact on your quality of life, and other factors specific to your case.

6. Who is eligible to file a Bard PowerPort lawsuit?

Individuals who were implanted with a Bard PowerPort device and subsequently experienced complications such as catheter fracture, infection, or blood clots may be eligible. Family members of patients who died from complications related to the device may also qualify to file a wrongful death claim.

7. What is the litigation process for a Bard PowerPort lawsuit?

The process typically begins with filing a complaint, followed by discovery (exchange of information), potential settlement negotiations, and if necessary, trial. Many medical device cases are resolved through settlements before reaching trial, but each case is unique.

8. How can I prove my injuries were caused by the Bard PowerPort device?

Medical records documenting the implantation of the device, subsequent complications, and treatment are essential. Expert testimony from medical professionals can also help establish the connection between the device and your injuries. An experienced attorney can help gather and present this evidence effectively.

See all related medical device lawsuits our lawyers have covered.

Get A Free Bard PowerPort Lawsuit Evaluation With Our Lawyers

Time is limited to pursue legal action for Bard PowerPort injuries. Many states have statutes of limitations of only 2-3 years from the date of injury or discovery of injury.

At Schmidt & Clark, LLP, we offer:

• Free, confidential consultations to evaluate your case
• No upfront costs or attorney fees
• Payment only if we win your case

Don’t delay seeking legal help for your Bard PowerPort injuries. Contact our experienced team today.

References:

1. https://dailyhornet.com/wp-content/uploads/2023/03/bard-powerport-lawsuit-patrice-t.pdf
2. https://www.aboutlawsuits.com/wp-content/uploads/2023-02-28-Complaint.pdf