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.
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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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Bard PowerPort device failure linked to Deep Vein Thrombosis (DVT).
Use the chatbot on this page to find out if you qualify for the Bard PowerPort Lawsuit.
On this page, we’ll discuss an overview of the Bard PowerPort Thrombosis Lawsuit, potential settlement amounts in Bard PowerPort lawsuits, who qualifies to file a Bard PowerPort Lawsuit, and much more.
The Bard PowerPort Device is a port catheter device used by a physician to access a patient’s bloodstream.
Otherwise known as Bard PowerPort catheters, Bard PowerPorts are the products of Bard Access Systems Inc., a medical device manufacturer based in Salt Lake City, Utah.
For years, the Bard PowerPort has been the go-to option for venous access.
However, victims have come forward, reporting various complications due to the device.
One of these complications associated with the Bard PowerPort is deep vein thrombosis (DVT) and blood clots.
If you or a loved one has suffered from deep vein thrombosis due to the Bard PowerPort Device, you may be eligible to join others filing Bard PowerPort Lawsuits.
Contact TorHoerman Law for a free case evaluation.
You can also use the chatbot on this page to find out if you qualify for the Bard PowerPort lawsuit instantly.
The Bard PowerPort Lawsuits aim to secure compensation for health problems and injuries linked to the medical device.
Reach out to our Bard PowerPort lawyers with any questions you may have about the lawsuit and the defective Bard PowerPort device.
The Bard Powerport is a type of port catheter developed and manufactured by Bard Access Systems Inc.
Bard PowerPort devices facilitate intravenous treatments, giving physicians an easy access point for drug infusions.
Due to the catheter’s placement on key blood vessels, Bard PowerPorts have also been used to obtain blood samples.
Implanting a Bard PowerPort is surgical, so the procedure is performed while the patient is under general or local anesthesia.
Physicians would select a suitable site based on the patient’s condition and incise near the site to create a subcutaneous pocket.
The subcutaneous pocket is where the physician would install the implant.
The physician then sutures the port catheter in place to prevent it from being dislodged.
Once installed, the Bard PowerPort device becomes the entry point for infusion systems.
Patients can then receive medications through the port catheter.
Port catheter devices are crucial medical tools that provide consistent and direct access to a patient’s vascular system, streamlining the administration of long-term treatments such as chemotherapy or frequent intravenous therapies.
Their design minimizes the need for repeated needle sticks, making treatments more comfortable for the patient while reducing potential complications from multiple venous punctures.
One of the features of port catheter devices is its ability to enhance the precision and efficiency of intravenous treatments.
For patients requiring therapies like chemotherapy, accurate administration of medications is highly important.
The Bard PowerPort aims to ensure that healthcare providers can precisely deliver medications and treatments, minimizing the margin for error.
This precision enhances the effectiveness of the treatment and contributes to a more targeted approach, potentially reducing side effects and improving overall outcomes.
Traditionally, repeated needle sticks for intravenous treatments can cause discomfort and anxiety for patients.
A port catheter device alleviates this burden significantly.
Once implanted, it provides a stable and easily accessible entry point for medical procedures.
The convenience of having a reliable access point just beneath the skin translates into a more comfortable experience, reducing the stress and apprehension often linked with regular medical treatments.
Prolonged use of traditional intravenous access methods can lead to vein damage, making it challenging for medical professionals to find suitable veins for future treatments.
Port catheters mitigate this concern by preserving the integrity of the patient’s veins.
With a catheter connected to a major vein, the wear and tear on peripheral veins are minimized.
This preservation of vein health ensures long-term access for necessary medical procedures.
It also enhances the patient’s overall vascular well-being, which is a crucial aspect for individuals undergoing extended treatment regimens.
Many patients and physicians have used the Bard PowerPort implantable port catheter, including:
Many patients have filed Bard PowerPort Lawsuits due to various complications arising from defective Bard PowerPort products.
Many of these complications occur as a result of catheter migration.
Catheter migration happens when the implant or a fragment of it breaks and travels to the bloodstream.
The Bard PowerPort device utilized a polyurethane and barium sulfate material to form the structure of the port catheter device.
Lawsuits claim that the polyurethane and barium sulfate particles can detach from the catheter, leading to an increased risk for catheter fracture and migration.
As the implant or fragment travels to numerous blood vessels, it can reach a bottleneck and obstruct blood flow.
With the blood flow obstructed, blood clots can develop and cause further blockage, leading to the following complications:
One of the complications potentially associated with defective Bard PowerPorts and catheter migration is deep vein thrombosis (DVT).
Deep vein thrombosis — commonly abbreviated as DVT — is a serious medical condition characterized by the formation of blood clots in deep veins, typically in the legs.
Blood clots impede normal blood flow, causing discomfort and posing severe health risks.
DVT can arise due to various factors, including prolonged immobility, genetic predisposition, or specific medical conditions.
It can also occur due to the presence of foreign objects like fragments from an implanted port catheter fracture.
DVT is a serious condition that requires prompt medical attention.
If left untreated, it can lead to more severe complications such as pulmonary embolism, where blood clots travels to the lungs, causing a potentially life-threatening situation.
DVT occurs when a blood clot forms in a deep vein.
In the context of the Bard PowerPort implant, the presence of the catheter inside a major vein can sometimes trigger the formation of these clots.
When an intravenous catheter, like those used with the Bard PowerPort, moves from its intended position, it can damage local vascular system walls.
This damage triggers the body’s clotting mechanism, leading to the formation of blood clots.
These clots can travel to various blood vessels.
Catheter-related DVT is a serious concern, especially for patients who are reliant on intravenous therapies.
Detecting and addressing catheter migration promptly is essential to prevent complications such as DVT.
Detecting DVT early is vital to prevent severe complications.
Common signs and symptoms of DVT include the following:
In the worst-case scenario, other signs and symptoms of DVT are sudden and unexplained shortness of breath and chest pain.
These indicate that a clot has traveled to the lungs, causing a potentially life-threatening condition known as pulmonary embolism.
Complications arising from DVT can be severe.
If a clot dislodges and travels to vital organs like the lungs, it can lead to pulmonary embolism, causing breathing difficulties and chest pain.
In some cases, DVT might result in chronic conditions like post-thrombotic syndrome, where severe and persistent pain and swelling occur on an affected leg.
Complications of deep vein thrombosis (DVT) include:
Prompt diagnosis and treatment of DVT are essential to minimize these complications and improve patient outcomes.
The primary goal of DVT treatment is to prevent the blood clot from growing larger and to stop it from breaking off and traveling to the lungs or other vital organs.
Common treatments and management approaches for DVT include:
Physicians will prescribe these treatments to continue for months.
Due to the duration of treatment, DVT management doesn’t just reduce a patient’s quality of life — the treatment can also be expensive.
Worse yet, these treatments of DVT don’t guarantee results.
In the worst-case scenario where part of a PowerPort implant has traveled to a blood vessel, surgical intervention may be necessary.
If a Bard PowerPort Device is the direct cause of DVT, surgical removal might be necessary.
Surgical removal involves a carefully planned procedure where the implant is extracted, eliminating the source of the clotting problem.
This intervention is crucial to prevent recurrent DVT episodes and to ensure the patient’s safety.
Surgical intervention can eliminate the root cause of blood clots.
Unfortunately, like most surgeries involving the vascular system, surgical removal may be life-threatening.
Complications from surgery can include:
When bleeding and post-operative infection aren’t addressed, a patient can go into shock.
Nerve damage from surgery may be extensive, potentially becoming irreversible.
Complications arising from a fractured and defective PowerPort can lead to life-threatening infections, shock, blood flow blockages, and even breathing problems from pulmonary embolism.
Injured patients are filing Bard PowerPort Lawsuits against the manufacturer.
If you or loved one were injured by a Bard PowerPort device, you may be eligible to file a Bard PowerPort Lawsuit.
Contact TorHoerman Law’s Bard PowerPort Lawyers for a free consultation.
You can also use the chatbot on this page to find out if you qualify to file a Bard PowerPort Lawsuit instantly.
Experienced Bard PowerPort lawyers will help victims throughout the legal process, completing steps such as gathering evidence and assessing damages.
Evidence is extremely important for product liability lawsuits, especially for lawsuits alleging defects on medical devices.
Your Bard PowerPort lawyer will help you gather evidence for your case.
Common Bard PowerPort lawsuit evidence includes:
Damages refer to the total amount of losses, economic and non-economic, incurred as a result of catheter failure.
Your lawyer will help you assess and calculate damages.
Potential Damages in a Bard PowerPort Lawsuit may include:
Our team of dedicated attorneys, with more than 100 years of combined litigation experience, have helped clients win more than $4 billion in verdicts and negotiated settlements for injuries suffered at no fault of their own.
If you or a loved one were injured by Bard PowerPort devices, you may be eligible to file a Bard PowerPort Lawsuit against the medical device manufacturer.
Contact TorHoerman Law for a free consultation.
You can also use the chatbot on this page to find out if you qualify for a Bard PowerPort Lawsuit instantly.
Our attorneys work on a contingency fee basis – so our clients don’t pay any legal fees unless they are awarded compensation for their injuries & other losses.
Reach out to us if you were injured by a defective device. We’re here to help you.
DVT is a serious condition where blood clots form in deep veins.
DVT can lead to severe complications if clots travel to vital organs like the lungs (pulmonary embolism).
When an intravenous catheter like the Bard PowerPort moves from its position, it can damage blood vessels, triggering clot formation.
Catheter-related DVT can be a result of this process.
Currently, the product liability lawsuits against Bard Access Systems Inc. have consolidated into multidistrict litigation (MDL).
MDL 3081 was filed in the U.S. District Court for the District of Arizona.
Multidistrict litigation (MDL) is a special federal legal procedure that allows cases alleging similar injuries from the same products or incidents to be centralized in a single US district court.
MDL is different and distinct from class action lawsuits.
In an MDL, plaintiffs retain their individuality and settlement compensation is distributed according to an individual’s circumstances and damages.
In a class action lawsuit, settlement compensation is distributed evenly amongst all claimants regardless of their individual circumstances.
The Bard PowerPort Lawsuit is still in its early stages and no settlements have been reached.
However, attorneys estimate that the average Bard PowerPort settlement may range between $10,000 to over $250,000 depending on an individual’s damages and the direction of the litigation.
These estimates are by no means a guarantee of compensation in the Bard PowerPort Lawsuit — they are merely projections based on results in past product liability lawsuits.
An experienced Bard PowerPort Lawyer can help determine if you qualify to file a Bard PowerPort Lawsuit and what to expect.
Contact TorHoerman Law for a free discussion about your legal options and the Bard PowerPort Lawsuit.
Visit this page to learn more about potential compensation in Bard PowerPort Lawsuits.
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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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.
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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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