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Bard Powerport Catheter® Devices: Seeking Justice and Compensation.
Those affected can request a 100% free private case evaluation.
Reports Claim that Bard® was aware that a large number of adverse event reports were filed with official agencies.
The main reason for a Bard PowerPort catheter implant is to provide long-term, repeated access to a patient’s veins for administering intravenous treatments, such as chemotherapy, blood transfusions, or medication.To know if you have a Bard PowerPort implant, look for a patient identification card/bracelet from your provider or feel for a triangular-shaped bump under the skin, usually on the right side of the chest below the collarbone .
The port has three raised "palpation bumps" on its top surface, which can be identified via imaging or physical touch.
How to Identify a Bard PowerPort:
- Documentation: Check the patient information packet, ID card, or bracelet provided at the time of insertion e.
- Physical Identification (Palpation): Gently feel under the skin. A PowerPort often feels triangular, and you can feel three small bumps on top of the silicone center .
- Imaging (X-ray): A trained clinician can confirm the port via X-ray, which will show a special symbol to confirm it is a power-injectable device i.
- "CT" Identifier: PowerPorts have the letters "CT" visible under X-ray m.
- Location: While most are in the chest (3-5 fingerbreadths below the collarbone), they can also be in the upper arm
One alleged victim, Ms. Nelk, filed a claim against the company. In the claim it is said that the company and defendants were aware that specific reports were made to health care providers of adverse events involving thromboembolism post-implantation & perforated internal vasculature, years before her PowerPort device was implanted.
Are you or a loved one facing difficulties due to Bard Powerport Catheter® devices? If so, you may be entitled to seek justice and compensation for the injuries and complications experienced. A dedicated team of experienced lawyers is here to help you navigate the legal process and fight for your rights. Our team understands the physical, emotional, and financial burdens caused by these devices, and we are committed to holding the responsible parties accountable.
Reports have surfaced regarding injuries and complications associated with Bard Powerport Catheter® devices:
- Device Dislodgement: Reports have emerged of the catheter device becoming dislodged from its intended position, which can lead to severe pain, internal damage, and the need for additional medical procedures.
- Infection and Sepsis: Patients have reported instances of infection and sepsis following the use of Bard Powerport Catheter® devices. These serious infections can result in life-threatening complications and require immediate medical attention.
- Blood Clots and Thrombosis: Some individuals have experienced blood clots and thrombosis due to the catheter device, leading to increased risks of heart attacks, strokes, and other cardiovascular complications.
- Device Malfunction and Breakage: Instances of device malfunction and breakage have been reported, causing significant harm to patients and necessitating further medical interventions.
- Organ Perforation: In certain cases, the Bard Powerport Catheter® device has been known to perforate nearby organs, resulting in severe pain, internal bleeding, and the need for emergency surgical intervention.
To know if you have a Bard PowerPort implant, look for a patient identification card/bracelet from your provider or feel for a triangular-shaped bump under the skin, usually on the right side of the chest below the collarbone .
The port has three raised "palpation bumps" on its top surface, which can be identified via imaging or physical touch.
How to Identify a Bard PowerPort:
- Documentation: Check the patient information packet, ID card, or bracelet provided at the time of insertion e.
- Physical Identification (Palpation): Gently feel under the skin. A PowerPort often feels triangular, and you can feel three small bumps on top of the silicone center .
- Imaging (X-ray): A trained clinician can confirm the port via X-ray, which will show a special symbol to confirm it is a power-injectable device i.
- "CT" Identifier: PowerPorts have the letters "CT" visible under X-ray m.
- Location: While most are in the chest (3-5 fingerbreadths below the collarbone), they can also be in the upper arm
If you or a loved one have suffered any of these injuries or complications due to Bard Powerport Catheter® devices, it's crucial to understand that you have legal options available. By filing a legal claim, you can seek justice and pursue compensation for the damages & injuries you have endured. It is important to have a skilled legal team that is prepared to assess your case, gather evidence, and build a strong legal strategy on your behalf.
We believe that those affected by medical device complications deserve fair compensation for their suffering, medical expenses, lost wages, and other related damages. We can also provide direct access to lawyers that have a deep understanding of product liability laws and are committed to advocating for your legal rights.
What is the Bard Powerport®?
The Bard PowerPort® device is a medical device used for the administration of medications, fluids, and blood products directly into a patient's bloodstream. It is a type of implanted port that consists of a small reservoir and a catheter. The device is surgically implanted under the skin, usually in the chest area, and connected to a vein.
What is the Bard Powerport® used for?
The PowerPort® device is primarily used in patients who require frequent or long-term intravenous therapies, such as chemotherapy, antibiotic treatment, or long-term intravenous nutrition. It provides a convenient and efficient way for healthcare providers to administer medications and fluids without the need for repeated needle sticks or peripheral IV access.
How does the Bard Powerport® Device work?
The device is accessed using a special needle that is inserted into the port, allowing healthcare professionals to deliver medications, draw blood samples, or perform other necessary procedures.
Take the first step towards justice and compensation today. Submit your information today for a 100% Free Case Evaluation.
Those who qualify may request a free, private case evaluation by a personal injury attorney!
Find Out if You Qualify
Bard Powerport Catheter Cases
Reports Claim that Bard® was aware that a large number of adverse event reports were filed with official agencies.
The main reason for a Bard PowerPort catheter implant is to provide long-term, repeated access to a patient’s veins for administering intravenous treatments, such as chemotherapy, blood transfusions, or medication.To know if you have a Bard PowerPort implant, look for a patient identification card/bracelet from your provider or feel for a triangular-shaped bump under the skin, usually on the right side of the chest below the collarbone .
The port has three raised "palpation bumps" on its top surface, which can be identified via imaging or physical touch.
How to Identify a Bard PowerPort:
- Documentation: Check the patient information packet, ID card, or bracelet provided at the time of insertion e.
- Physical Identification (Palpation): Gently feel under the skin. A PowerPort often feels triangular, and you can feel three small bumps on top of the silicone center .
- Imaging (X-ray): A trained clinician can confirm the port via X-ray, which will show a special symbol to confirm it is a power-injectable device i.
- "CT" Identifier: PowerPorts have the letters "CT" visible under X-ray m.
- Location: While most are in the chest (3-5 fingerbreadths below the collarbone), they can also be in the upper arm
One alleged victim, Ms. Nelk, filed a claim against the company. In the claim it is said that the company and defendants were aware that specific reports were made to health care providers of adverse events involving thromboembolism post-implantation & perforated internal vasculature, years before her PowerPort device was implanted.
Are you or a loved one facing difficulties due to Bard Powerport Catheter® devices? If so, you may be entitled to seek justice and compensation for the injuries and complications experienced. A dedicated team of experienced lawyers is here to help you navigate the legal process and fight for your rights. Our team understands the physical, emotional, and financial burdens caused by these devices, and we are committed to holding the responsible parties accountable.
Reports have surfaced regarding injuries and complications associated with Bard Powerport Catheter® devices:
- Device Dislodgement: Reports have emerged of the catheter device becoming dislodged from its intended position, which can lead to severe pain, internal damage, and the need for additional medical procedures.
- Infection and Sepsis: Patients have reported instances of infection and sepsis following the use of Bard Powerport Catheter® devices. These serious infections can result in life-threatening complications and require immediate medical attention.
- Blood Clots and Thrombosis: Some individuals have experienced blood clots and thrombosis due to the catheter device, leading to increased risks of heart attacks, strokes, and other cardiovascular complications.
- Device Malfunction and Breakage: Instances of device malfunction and breakage have been reported, causing significant harm to patients and necessitating further medical interventions.
- Organ Perforation: In certain cases, the Bard Powerport Catheter® device has been known to perforate nearby organs, resulting in severe pain, internal bleeding, and the need for emergency surgical intervention.
If you or a loved one have suffered any of these injuries or complications due to Bard Powerport Catheter® devices, it's crucial to understand that you have legal options available. By filing a legal claim, you can seek justice and pursue compensation for the damages & injuries you have endured. It is important to have a skilled legal team that is prepared to assess your case, gather evidence, and build a strong legal strategy on your behalf.
We believe that those affected by medical device complications deserve fair compensation for their suffering, medical expenses, lost wages, and other related damages. We can also provide direct access to lawyers that have a deep understanding of product liability laws and are committed to advocating for your legal rights.
What is the Bard Powerport®?
The Bard PowerPort® device is a medical device used for the administration of medications, fluids, and blood products directly into a patient's bloodstream. It is a type of implanted port that consists of a small reservoir and a catheter. The device is surgically implanted under the skin, usually in the chest area, and connected to a vein.
What is the Bard Powerport® used for?
The PowerPort® device is primarily used in patients who require frequent or long-term intravenous therapies, such as chemotherapy, antibiotic treatment, or long-term intravenous nutrition. It provides a convenient and efficient way for healthcare providers to administer medications and fluids without the need for repeated needle sticks or peripheral IV access.
How does the Bard Powerport® Device work?
The device is accessed using a special needle that is inserted into the port, allowing healthcare professionals to deliver medications, draw blood samples, or perform other necessary procedures.
Take the first step towards justice and compensation today. Submit your information today for a 100% Free Case Evaluation.
Those who qualify may request a free, private case evaluation by a personal injury attorney!
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A qualified legal team led by a personal injury attorney will consider the facts of the case and the potential for compensation.
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Those that qualify will have an individual claim filed in a court of law for the justice and compensation they deserve.
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We believe that victims of the Bard Powerport Catheter® warming system and the families that lost members deserve both compensation and justice starting with a free, private case evaluation.
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