You may be eligible to file a Tylenol Autism ADHD Lawsuit / Acetaminophen Autism ADHD Claim if you or a loved one used Tylenol and/ or Acetaminophen during pregnancy, and your child was subsequently diagnosed with ADHD or Autism Spectrum Disorder.
Legal action is being strategized by our attorneys for Horizon Therapeutics’ failure to properly warn patients of potential hearing loss side effects.
You may be eligible to file a Tepezza Lawsuit if you or a loved one took Tepezza and subsequently suffered permanent hearing loss or tinnitus.
If you or a loved one took Elmiron and subsequently suffered vision loss, blindness, or any other eye injury linked to the prescription drug.
Contact the Elmiron Lawyers from TorHoerman Law.
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You may qualify to participate in a 3M Combat Arms Earplugs Lawsuit if:
Over 140,000 Exactech hip, knee and ankle implants have been recalled due to packaging errors that can lead to the breakdown of parts vital to the device’s function.
If you or a loved one suffered injuries from an Exactech implant device, you may be entitled to financial compensation.
You may be eligible to file a Hair Straightener Cancer Lawsuit if you or a loved one used chemical hair straighteners, hair relaxers, or other similar hair products, and subsequently were diagnosed with:
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Over one million people, who were present at Camp Lejeune (North Carolina) between 1953 and 1987, may have been exposed to toxic substances in the water.
The Camp Lejeune Contaminated Water Lawsuit can apply to you, a family member, or a loved one who lived at Camp Lejeune (North Carolina) and suffered health effects from the decades of water contamination that occurred.
Toxic chemicals in Aqueous Film-Forming Foam (AFFF Firefighting Foam) have been linked to numerous types of cancer, including:
AFFF Firefighting Foam lawsuits aim to hold manufacturers accountable for putting peoples’ health at risk.
If you have been exposed to Paraquat and diagnosed with Parkinson’s disease may be eligible to pursue compensation, and entitled to participate in the paraquat lawsuit.
Contact us today to see if you qualify for the Paraquat Parkinson’s Disease Lawsuit!
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Our firm is about people. That is our motto and that will always be our reality.
We do our best to get to know our clients, understand their situations, and get them the compensation they deserve.
At TorHoerman Law, we believe that if we continue to focus on the people that we represent, and continue to be true to the people that we are – justice will always be served.
Without our team, we would’nt be able to provide our clients with anything close to the level of service they receive when they work with us.
The THL Team commits to the sincere belief that those injured by the misconduct of others, especially large corporate profit mongers, deserve justice for their injuries.
Our team is what has made TorHoerman Law a very special place since 2009.
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Learn more about injuries and complications of the Bard Implantable Port Device.
Contact us to find out if you qualify for the Bard PowerPort Lawsuit.
The Bard PowerPort Implantable Port Device is a medical device used to deliver medications into the bloodstream.
It has been linked to various complications and injuries, some of which can be severe.
Other serious injuries that can occur include air embolism, allergic reaction, and cardiac arrhythmia.
Question: What injuries are linked to the Bard PowerPort Implantable Port Device?
Answer: The Bard PowerPort implantable port device has been linked to several serious injuries.
These injuries include, but are not limited to catheter fractures, catheter migration, deep vein thrombosis (DVT), damage to veins and blood vessels, catheter infection, blood vessels necrosis, blood clots, and arterial puncture.
On this page, we’ll discuss this question in further depth, an overview of what the Bard PowerPort implantable port device is, the risks and complications associated with it, and much more.
In recent years, concerns have arisen regarding the safety of the Bard PowerPort implantable port device.
Patients who have undergone implantation of this medical device have reported various complications and injuries associated with its use.
Injuries linked to the defective Bard Power Port catheter device include catheter failure, fracture, migration, blood clots, deep vein thrombosis, and more.
Injured patients are filing lawsuits against the medical device company.
Bard PowerPort Lawsuits claim that the use of this implantable catheter port device results in an increased risk for severe injuries.
If you or a loved one has suffered from any of these complications after receiving a Bard PowerPort implantable port, you may be eligible to file a Bard PowerPort Lawsuit.
Contact TorHoerman Law today for a free consultation.
You can also use the chatbot on this page to find out if you qualify for the Bard PowerPort lawsuit instantly.
Our Bard PowerPort lawyers have decades of experience securing compensation for people filing product liability lawsuits.
We understand the impacts that these injuries can have on a patient’s quality of life, and we are committed to representing individuals harmed at no fault of their own.
If your PowerPort fractured or otherwise injured you, reach out to our PowerPort lawyers today.
Bard PowerPort devices, designed to facilitate the administration of medications, fluids, and blood products, have been associated with several serious injuries and complications.
Complications, injuries, and adverse health effects linked to the defective port catheters include:
Catheter migration is a significant concern associated with the Bard PowerPort catheters.
Catheter migration occurs when the catheter tube, a thin tube that connects the port to a larger vein, shifts from its intended position.
When catheter migration happens, it can lead to several complications, including:
Catheter fracture is another severe issue associated with the Bard PowerPort device.
This situation occurs when the catheter, which is typically made of flexible material, breaks or snaps.
The consequences of catheter fracture include:
Deep vein thrombosis (DVT) is a severe condition where blood clots form within deep veins, usually in the legs.
In the context of the Bard PowerPort device, thrombosis can occur around the catheter or in the blood vessels connected to the port.
Complications associated with thrombosis include:
Infections related to the defective Bard PowerPort device are a significant concern.
Cracks, fissures, and fractures on the port catheter device can increase the risk for infection.
Infections can lead to a range of health issues, including:
In addition to the injuries mentioned above, patients have reported other complications associated with the Bard PowerPort catheter device.
Additional Bard PowerPort complications and injuries include:
The Bard PowerPort is a medical device designed to simplify the process of administering medications, chemotherapy, and drawing blood for patients who require frequent intravenous (IV) treatments.
The Bard PowerPort is a small implantable port-catheter system that enhances medical care and patient comfort.
The Bard PowerPort device, manufactured by Bard Access Systems, Inc. (a subsidiary of Becton Dickinson and Company), is a type of vascular access device.
It is a small, round, flat implantable port placed beneath the skin, typically in the upper chest area.
The device includes a self-sealing septum and a catheter that connects to a major vein, such as the subclavian or jugular vein.
The primary purpose of the Bard PowerPort device is to provide a reliable and convenient means for healthcare providers to access a patient’s vascular system.
This access is essential for various medical procedures, including:
The Bard PowerPort is primarily useful for patients who require long-term or frequent IV treatments.
Individuals who may use the PowerPort includes, but is not limited to:
While the port catheter devices have been instrumental in improving the quality of care for many patients, there have been reported issues and complications associated with certain models.
Several adverse event reports have reached the U.S. Food and Drug Administration (FDA) regarding complications related to the Bard PowerPort medical devices.
On March 26, 2020, the FDA issued a Class II recall for certain Bard PowerPort devices, which contained the wrong tunneler tips.
This error could affect the placement of the device and lead to severe complications.
Additionally, the FDA Manufacturer and User Facility Device Experience (MAUDE) database contains numerous reports of complications associated with Bard PowerPort devices, including malfunctions and injuries.
On February 18, 2022, the FDA terminated the Bard PowerPort recall, and there are currently no active recalls for these medical devices.
However, patients and healthcare providers should remain aware of potential complications and promptly report any issues to the FDA.
In response to the reported injuries and complications associated with the Bard PowerPort device, multiple plaintiffs filed Bard PowerPort lawsuits against Bard Access Systems, Inc.
Aside from the medical device manufacturer, its parent company, Becton Dickinson and Company, is also a primary defendant in these lawsuits.
The Bard PowerPort Lawsuit allegations focus on three main issues:
Additionally, the Bard PowerPort lawsuits allege that the company was aware of design defects in their devices but failed to take appropriate action, putting patients at risk.
There are 50 Bard PowerPort lawsuits consolidated into multidistrict litigation (MDL) in the U.S. District Court for the District of Arizona.
Judge David G. Campbell presides over MDL 3081, allowing for a more efficient and streamlined legal process for similar lawsuits.
As the Bard PowerPort lawsuits progress, lawyers estimate that the average Bard PowerPort settlement could range from $10,000 to $100,000.
However, the final settlement amount will depend on various factors, such as the severity of injuries and individual circumstances.
These estimations for Bard PowerPort settlement amounts are merely projections and are not a guarantee of financial compensation in the Bard PowerPort Lawsuit.
Visit this page for more information on projected Bard PowerPort Lawsuit settlement amounts.
Individuals who have experienced injuries or complications related to the Bard PowerPort device may qualify for legal action if they meet specific criteria.
Potential plaintiffs in Bard PowerPort Lawsuits may include:
It is essential to consult with a qualified Bard PowerPort injury lawyer to determine if you are eligible for legal action and to understand your rights and options.
At Torhoerman Law, our team of experienced Bard PowerPort injury lawyers can evaluate your case and help guide you through the legal process.
We understand the toll that these medical devices can have on individuals and their families, and we are dedicated to fighting for your rights.
If you or a loved one has experienced adverse events, injuries, or other complications associated with the Bard PowerPort device, you may be eligible to file a Bard PowerPort Lawsuit.
Contact TorHoerman Law today for a free consultation.
You can also use the chatbot on this page to find out if you qualify for the Bard PowerPort lawsuit instantly.
Reach out to our Bard PowerPort Lawyers for more information and to ask any questions you may have about the Bard PowerPort device.
The Bard PowerPort is an implantable port-catheter system designed to provide access to a patient’s bloodstream for administering medications and collecting blood samples.
The Bard PowerPort device is commonly used in patients with cancer undergoing chemotherapy, individuals requiring long-term intravenous therapy, or those who need frequent blood draws.
Injuries linked to the Bard PowerPort device include catheter migration, catheter fracture, infection, and thrombosis.
These complications can lead to pain, discomfort, and other health issues.
The Bard PowerPort is currently not recalled.
Bard has issued multiple recalls in the past for different versions of the Bard PowerPort device due to concerns about catheter failure and other issues.
The FDA has also issued warnings and safety communications related to this device.
Individuals who have experienced injuries or complications related to the Bard PowerPort device and families of deceased patients may qualify for legal action.
It’s advisable to consult with an attorney specializing in medical device litigation to assess eligibility.
No, there is not a Bard PowerPort class action lawsuit.
Bard PowerPort Lawsuits are consolidated into multidistrict litigation (MDL).
MDL is a special federal legal procedure that allows for cases alleging similar injuries and facts to be centralized in a single US District Court.
MDL is different from a class action lawsuit.
In the event of a settlement in an MDL, compensation is distributed to claimants according to the facts and circumstances of their individual lawsuits.
In a class action lawsuit, settlement compensation is divided evenly among all claimants regardless of their individual circumstances.
Owner & Attorney - TorHoerman Law
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
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In this case, we were able to successfully recover $20 Million for our client after they suffered a Toxic Tort Injury due to chemical exposure.
In this case, we were able to successfully recover $103.8 Million for our client after they suffered a COX-2 Inhibitors Injury.
In this case, we were able to successfully recover $4 Million for our client after they suffered a Traumatic Brain Injury while at daycare.
In this case, we were able to successfully recover $2.8 Million for our client after they suffered an injury due to a Defective Heart Device.
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
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You can learn more about the Bard PowerPort Lawsuit by visiting any of our pages listed below:
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