Catheter-Related Bloodstream Infections (CRBSIs) Attorney

Catheter-related bloodstream infections (CRBSIs) are a significant concern in medical practice, particularly for patients requiring prolonged catheter use. These infections can have severe, even life-threatening consequences. One medical device linked to an increased risk of CRBSIs is the Bard Power Cord, a vascular access device used in medical settings.

At Jeffrey Glassman Injury Lawyers, we are dedicated to protecting the rights of individuals harmed by defective medical devices. We explore CRBSIs, the risks associated with Bard Power Cords, and the legal recourse available to affected individuals.

CRBSIs occur when bacteria or fungi enter the bloodstream through an indwelling catheter, a tube inserted into a vein to deliver medications, fluids, or nutrition. Central venous catheters (CVCs), such as the Bard Power Cord, are often used for patients undergoing long-term treatments like chemotherapy, dialysis, or parenteral nutrition.

CRBSIs are considered preventable if proper hygiene protocols and device design are followed. However, faulty or poorly designed medical equipment can significantly elevate the risk of infection.

The Bard Power Cord is a type of CVC widely used in healthcare settings. While it offers convenience for medical professionals and patients, its design and manufacturing have been associated with complications, including CRBSIs.

1. Material Defects: The device's materials may harbor bacteria or degrade over time, increasing the likelihood of infection.
2. Insertion Challenges: If the catheter is difficult to insert or becomes dislodged, it can create micro-tears in the vein, providing an entry point for bacteria.
3. Design Flaws: Complex designs may make thorough cleaning difficult, leaving patients vulnerable to infection.

Healthcare professionals and patients have raised concerns about the Bard Power Cord's ability to maintain sterility over extended periods, putting patients at significant risk of CRBSIs and related complications.

CRBSIs can escalate rapidly, making early detection and treatment essential. Common symptoms include:

• Fever and chills
• Redness or swelling at the catheter insertion site
• Pain around the catheter site
• Low blood pressure in severe cases
• Septic shock, if untreated

The complications of CRBSIs can range from prolonged hospital stays and organ failure to, in severe cases, death.

The risks associated with Bard Power Cords have prompted investigations and legal actions. Allegations include:

• Defective Design: Claims that the device’s design increases susceptibility to CRBSIs.
• Manufacturing Negligence: Instances where poor manufacturing standards led to contaminated devices.
• Inadequate Warnings: Bard's failure to adequately inform healthcare providers and patients about the infection risks linked to their product.

Patients who suffered CRBSIs after using Bard Power Cords may be entitled to compensation for their injuries, including medical expenses, lost wages, and pain and suffering.

Several lawsuits have been filed against medical device manufacturers, including Bard, for complications stemming from defective products. These cases often focus on whether the company knew the risks and failed to take appropriate action. Key elements typically examined in these lawsuits include:

1. Evidence of Negligence: Documentation of defects or prior complaints about the product.
2. Causation: Medical evidence linking the infection to the device.
3. Damages: The financial and emotional toll on the affected individual.

For example, lawsuits involving CRBSIs have highlighted the devastating impact on patients, some of whom faced life-threatening conditions due to infections directly linked to defective catheters.

If you or a loved one has suffered a CRBSI after using a Bard Power Cord, it is crucial to act promptly. Here are steps to protect your rights and health:

1. Seek Immediate Medical Attention: Ensure a healthcare professional treats and documents your infection.
2. Preserve Evidence: Retain the Bard Power Cord and related medical records as evidence.
3. Consult an Experienced Attorney: Legal professionals familiar with medical device litigation, like Jeffrey Glassman Injury Lawyers, can evaluate your case and guide you through the legal process.

At Jeffrey Glassman Injury Lawyers, we understand the complexities of medical device litigation. We are dedicated to holding manufacturers accountable for negligence and securing justice for individuals harmed by defective products.

• Thorough Investigation: We analyze every aspect of your case, including medical records, device design, and manufacturer history.
• Expert Partnerships: Collaborating with medical experts, we build strong arguments to establish causation and liability.
• Client-Centered Advocacy: Your well-being is our priority, and we work tirelessly to achieve the best possible outcome for you.

Our team has a proven track record of securing compensation for clients affected by medical negligence and defective devices.

Medical device manufacturers have a responsibility to prioritize patient safety. When companies cut corners or fail to address known risks, they endanger lives. Legal action relieves victims and compels manufacturers to improve safety standards, potentially preventing future harm.

CRBSIs caused by defective devices like the Bard Power Cord represent a serious public health issue. If you or someone you know has experienced a catheter-related bloodstream infection linked to a Bard product, you have the right to seek justice and compensation. At Jeffrey Glassman Injury Lawyers, we are here to help. Our experienced team is ready to stand by your side, fight for your rights, and hold negligent manufacturers accountable.

Contact us today for a free consultation at (617) 777-7777 to discuss your case and explore your legal options.

Your health and well-being are too important to leave to chance. Let us help you take the first step toward justice and recovery.