Seek medical attention immediately, document your symptoms and medical treatments, and consult an attorney to discuss your options.
Bard PowerPort medical devices are meant to ease treatment and improve outcomes for patients who require frequent intravenous treatments.
But for many patients, these devices have caused pain and suffering. Severe complications like infections, blood clots, and migration of device material have all been reported due to the barium sulfate in the catheter.
If you or your loved ones have suffered due to Bard PowerPort, you deserve justice for the unnecessary risks and pain caused by this defective device.
If you or a loved one have suffered from Bard PowerPort complications, contact us to schedule a free case evaluation.
Join hundreds of others who have stood up against Bard PowerPort’s negligence. Together, we can make a difference.
In August 2023, these lawsuits were consolidated into federal multidistrict litigation (MDL) No. 3081, which is now being overseen by Judge David G. Campbell in the U.S. District Court for Arizona.
Taking action in an MDL means your case will be part of a large, coordinated effort. This strategy is intended to hopefully help clients obtain settlements with lower legal costs, and more consistent trial outcomes.
An MDL allows many cases with similar claims against the same defendant to be handled together. This strategy is similar to a class action lawsuit, but each patient’s case remains individual, recognizing each person’s unique experience.
As of July 9, 2024, there are 322 cases pending in the Bard PowerPort MDL, with additional cases in the Superior Court of New Jersey.
Plaintiffs of the Bard implant lawsuit have made these legal claims
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Product liability |
Negligence |
Failure to warn |
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1) Defective Bard PowerPort catheters contain a high concentration of barium sulfate, causing lower material integrity. Resulting fractures or migrations of the catheter have led to significant injuries. |
2) Because of their high failure rate, these devices should not have been marketed as safe. The manufacturer bears responsibility for this negligence. |
3) The manufacturer did not effectively and swiftly warn healthcare providers and patients about the device’s risks. As a result, neither providers nor patients were given the information they needed to consider alternatives. |
With extensive experience pursuing MDL and defective device claims, Stark & Stark’s Bard PowerPort defect attorneys are here to help. Reach out today to start the process.
The complaints brought so far involve over a dozen models of the device, including:
You trusted Bard PowerPort for your health. Let us help you hold them accountable for breaking that trust. Contact our experienced MDL legal team for a free case evaluation.
You may be eligible to join the Bard PowerPort litigation if you:
Family members of deceased patients may also file wrongful death claims if there is proof the device contributed to your loved one’s death.
Let us help you hold the responsible parties accountable for your injuries. Contact a Stark & Stark Bard PowerPort injury lawyer today for a free case evaluation.
Patients have a Bard device surgically placed into one of the large central veins that takes blood to the heart. This device allows medicine and fluids to be given and blood samples to be taken directly through the port, reducing the need for multiple needle sticks.
Under ideal circumstances, this would offer a convenient, less painful option for patients undergoing long-term treatments.
No one should endure more pain from a device meant to help. Yet, that’s the reality for Bard PowerPort patients who have suffered complications, injuries, and ultimately more medical costs after installation.
These serious injuries often result from the Bard PowerPort’s faulty design. In some cases, particles from the catheter have broken free (fractured) and moved through the body. Others are due to the device’s migration (movement) within the body.
Discuss your injuries and find out if you qualify for compensation. Schedule a free case evaluation with one of Stark & Stark’s knowledgeable defective device attorneys.
The first step to filing a lawsuit is to collect any information that might be relevant. In this case, potential claimants should gather as many of the following as possible:
The next step is to contact an experienced Bard PowerPort defect attorney. They can help you understand your options for pursuing compensation for your pain and suffering.
You shouldn’t have to face this alone. We’re here to provide the compassionate, one-on-one support you need.
At Stark & Stark, we have deep knowledge of the ins and outs of product liability and medical device defect cases needed to pursue Bard Powerport injury claims effectively. We’ll ensure your case is thoroughly investigated and, if eligible to file, represented robustly for the best chance at compensation.
Take the first step toward filing your Bard catheter lawsuit now and hold those responsible accountable.
What do I do if I suspect my medical device is defective?
Seek medical attention immediately, document your symptoms and medical treatments, and consult an attorney to discuss your options.
How much money could I receive in a Bard PowerPort settlement?
This is something that will depend on injury severity, s0 speaking with an attorney to better understand your case is always the best course of action.
How long do patients have to file PowerPort injury claims?
It’s crucial to contact an attorney promptly because statutes of limitations may apply. Delaying action could result in losing your right to seek compensation.
Is there a Bard PowerPort recall?
No. The manufacturer has not issued a recent voluntary recall related to the lawsuit, and the FDA has not required one at this time.
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