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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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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Bard PowerPort catheter infection can result in serious injuries and complications.
Use the chatbot on this page to find out if you qualify for the Bard PowerPort Lawsuit.
Bard has been accused of not adequately warning patients about the risks associated with their device.
If you have been injured by a Bard PowerPort device, you may be eligible to file a lawsuit and seek compensation.
Bard has been accused of not adequately warning patients about the risks associated with their device.
On this page, we will provide an overview of the Bard PowerPort Catheter Infection Lawsuit, alleged catheter device defects, the legal implications of the defects, and much more.
An implantable port catheter device can be a vital and life-changing medical device for patients who require intravenous fluids.
The Bard PowerPort device is used to gain access to a patient’s vascular system, but recent lawsuits claim that the Bard PowerPort device may be linked to serious injuries and complications.
A combination of polyurethane and barium sulfate materials used on the device (known as Chronoflex AL), may be prone to breaking or fracturing, leading to complications such as device migration and catheter infections.
We will discuss catheter infections, why they may occur with Bard PowerPort devices, potential Bard PowerPort complications, and answer frequently asked questions about these lawsuits.
If you or a loved one were injured by a Bard PowerPort Device, you may be eligible to file a Bard PowerPort Lawsuit and seek compensation.
Contact TorHoerman Law 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 are here to help victims through the legal process and advocate on their behalf for compensation.
Reach out to us with any questions you may have about Bard PowerPort complications, Bard PowerPort Lawsuits, and more.
We are here for you.
The Bard PowerPort, manufactured by Bard Access Systems Inc., is a medical device designed to provide access to a patient’s bloodstream.
This access point is critical in modern medicine, allowing healthcare professionals to perform various medical procedures.
The Bard PowerPort consists of a small chamber and catheter surgically implanted beneath the patient’s skin.
The catheter is then threaded into a large vein, typically in the chest, as a conduit for administering drugs, fluids, or blood products.
This device is widely used in cancer treatment, long-term antibiotic therapy, and other medical conditions that require frequent intravenous access.
Bard PowerPort devices are primarily used by patients who require long-term intravenous therapy or frequent access to their veins.
Patients who use the Bard PowerPort device may include:
The convenience and supposed reliability of the Bard PowerPort device have made it an attractive option for healthcare providers and patients seeking a more comfortable and efficient means of delivering crucial treatments.
While the Bard PowerPort catheter device has been widely used in the healthcare industry to streamline intravenous access for countless patients, it has not been immune to complications.
Among the most pressing concerns is the device’s propensity to a catheter fracture and crack.
This vulnerability can pave the way for infections and various other health issues, including:
Catheter infections represent a substantial and potentially life-threatening complication of Bard PowerPort devices.
Catheter infections manifest at or near the site where a catheter tube is inserted into the body, and within the context of Bard PowerPort devices, they can develop within the fissures and cracks that may form in the catheter or its surrounding components.
Possible complications of catheter infections include:
The occurrence of catheter infections in conjunction with Bard PowerPort devices can be attributed to a combination of factors.
The main reasons for catheter infections related to the Bard PowerPort device revolve around the material with which the device is manufactured.
Bard PowerPort devices are produced using Chronoflex AL, a material comprised of a mixture of polyurethane and barium sulfate.
This material has the potential to break away from the catheter body, resulting in fragmentation, cracks, fissures, and other defects on the port catheter device.
Infections can manifest within the cracks of the port catheter device, leading to complications.
The materials used in the construction of Bard PowerPort devices, while chosen for their biocompatibility, strength, and durability, are not impervious to the rigors of long-term use within the human body.
Over time, these materials may undergo wear, tear, and degradation.
Such structural compromises render them more susceptible to developing cracks or fissures, which, unfortunately, can serve as breeding grounds for bacteria.
While not immediately apparent, this material vulnerability poses a significant risk to patients who rely on Bard PowerPort devices for continuous medical care.
These microscopic openings provide opportunistic pathogens with a route to access blood vessels, thereby increasing the likelihood of infection.
The presence of a catheter within the body, although medically necessary, represents an inherent foreign body.
In essence, it creates an artificial passage into the bloodstream.
This entry point can be exploited by bacteria and other microorganisms.
While typically sterile upon insertion, this foreign body is not immune to contamination, especially in the presence of the aforementioned material vulnerabilities.
When the catheter’s integrity is compromised through fracturing or cracking, it becomes a beacon for bacteria, allowing them to enter and colonize the area.
This can set the stage for infection, blood clots, and deep vein thrombosis, potentially leading to grave consequences if not promptly addressed.
Many patients requiring Bard PowerPort devices do so for extended periods, sometimes several months or even years.
While these devices offer the advantage of consistent intravenous access, this extended duration of placement also increases the susceptibility to infections over time.
The longer a Bard PowerPort device remains in place, the greater the opportunity for contaminants to infiltrate the system, potentially leading to serious injuries and conditions.
Catheter infections, while often underestimated, can have far-reaching and profound consequences for patients, affecting their physical health and overall well-being.
The complexities and potential severity of these health complications deserve a comprehensive examination.
Among the most critical complications stemming from catheter infections are systemic infections, which pose a grave risk to patients.
These infections, originating from catheter-related complications, can rapidly spread throughout the body.
Sepsis, a life-threatening condition, represents the ultimate consequence of unchecked systemic infections.
It is characterized by widespread inflammation, organ dysfunction, and a heightened risk of mortality.
When infections infiltrate the bloodstream via catheter-related issues, they can provoke an uncontrolled immune response, sending the body into a state of crisis.
Organs may begin to fail, leading to a dire medical emergency. Sepsis requires immediate and aggressive medical intervention, often involving intensive care and treatment with antibiotics and other medications.
Infections localized at the catheter insertion site can inflict significant discomfort and distress upon patients.
This localized inflammation can manifest as pain, swelling, redness, and irritation, impairing the patient’s quality of life.
Pain can be incredibly disruptive, interfering with daily activities and hindering the effectiveness of ongoing treatment.
Additionally, the physical discomfort can take a toll on a patient’s emotional well-being, further complicating the healing process.
Catheter infections not only jeopardize the patient’s health but also compromise the very functionality of the Bard PowerPort device itself.
When an infection takes hold, it can impede the device’s operation, hindering the delivery of critical medications, fluids, or other essential treatments.
In some cases, the device may become entirely inoperative, necessitating its removal or replacement.
Removing or replacing an infected Bard PowerPort device introduces additional medical procedures and disruptions to the patient’s healthcare journey.
This translates to increased physical and emotional strain on the patient and potential delays in receiving necessary treatments.
Severe infections stemming from Bard PowerPort catheters often mandate extended hospital stays and intensive treatment.
These prolonged hospitalizations impose a multifaceted burden on patients and their families.
In addition to the physical toll, they can be emotionally taxing, leading to anxiety and distress.
Moreover, the financial implications of extended hospitalization can be overwhelming, further exacerbating the challenges faced by patients and their loved ones.
The increasing incidence of catheter infections, fractures, and migration linked to Bard PowerPort devices has ignited a wave of legal actions as patients and their families seek accountability for the harm they have endured.
Bard PowerPort Lawsuits filed against the manufacturer, Bard Access Systems Inc., are founded on the assertion that the company inadequately warned healthcare providers and patients about the potential risks associated with their product.
The emergence of catheter-related infections as a significant concern within the Bard PowerPort user community has set off alarm bells within the healthcare industry and beyond.
Some patients who initially sought the convenience and benefits of Bard PowerPort devices have been confronted with the distressing reality of catheter-related infections, which can range from painful local complications to life-threatening systemic conditions.
In response to the growing number of catheter infections and the perceived lack of transparency regarding the risks, lawsuits have been initiated against Bard Access Systems, the manufacturer of Bard PowerPort devices.
These legal actions are grounded in several key allegations.
One of the primary contentions in these lawsuits is that Bard Access Systems failed to adequately warn healthcare providers and patients about the potential risks of Bard PowerPort implantable port devices.
Plaintiffs argue that comprehensive and transparent disclosure of the device’s vulnerabilities, including the susceptibility to fractures and the consequent risk of infections, would have empowered healthcare providers and patients to make informed decisions about its use.
Plaintiffs assert that the manufacturer, Bard Access Systems, demonstrated negligence in the design, manufacturing, and marketing of the Bard PowerPort implant.
They contend that the device’s material vulnerabilities and propensity for fractures should have been addressed more proactively and that the company failed to implement adequate safety measures to mitigate these risks.
The individuals and families pursuing Bard PowerPort Lawsuits are motivated by justice, accountability, and, most importantly, patient safety.
We believe that the healthcare industry, including medical device manufacturers, must uphold the highest standards of well-being and transparency to protect the well-being of patients.
Filing lawsuits serve not only as a means of seeking compensation for the physical, emotional, and financial toll imposed by catheter-related infections but also as a catalyst for change within the medical device industry.
By holding manufacturers accountable for their products’ safety and ensuring that healthcare providers and patients are adequately informed about potential risks, Bard PowerPort Lawsuits strive to prevent future cases of unnecessary suffering.
The Bard PowerPort Catheter Infection Lawsuit highlights the challenges faced by patients who have experienced catheter infections due to using this medical device.
While port catheters have been a valuable tool in medical treatment, the susceptibility to infections due to material vulnerabilities in Bard PowerPort devices has raised serious concerns.
Patients affected by these infections are seeking justice through lawsuits to hold the manufacturer accountable for the harm they have endured.
If you or a loved one has been injured by a Bard PowerPort device, you may be eligible to file a Bard PowerPort Lawsuit.
Contact TorHoerman Law for a free consultation.
You can use the chatbot on this page to determine if you qualify for the Bard PowerPort Lawsuit instantly.
A Bard PowerPort injury lawyer can provide guidance and support during this difficult time, in the pursuit of fair compensation and accountability.
Reach out to our team with any questions you may have about the Bard PowerPort Lawsuit.
If you have had a Bard PowerPort device implanted for intravenous therapy, it should be documented in your medical records.
You can also contact your healthcare provider for information about your implantable port.
Common signs of a catheter infection include redness, swelling, severe and persistent pain, or tenderness at the catheter insertion site, fever, chills, and discharge from the site.
If you experience any of these symptoms, seek medical attention immediately.
If you believe you have suffered harm due to a Bard PowerPort catheter infection, consult an experienced attorney specializing in medical device litigation.
They can evaluate your case and guide you through the legal process.
You can use the chatbot on this page to find out if you qualify for the Bard PowerPort Lawsuit instantly.
Bard Access Systems Inc. has faced lawsuits alleging that they did not adequately warn about the risks associated with their Bard PowerPort devices.
Other lawsuits have been filed against Bard for defects and injuries related to their IVC Filters.
Patients who have suffered harm due to Bard PowerPort catheter infections may be eligible for compensation through lawsuits or settlements.
Consulting with a Bard PowerPort lawyer is advisable to explore your legal options.
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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Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
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