Patients Raise Concerns Over Safety of Bard PowerPort Cather

What is the Bard PowerPort

Bard PowerPort, also known as an implantable venous device, is manufactured by Bard Access Systems, which is a subsidiary company of Becton, Dickinson and Company. These devices provide long-term IV access and allow for repeated medication, fluids, blood product delivery, as well as blood sample collection.

PowerPorts and other devices of the same type are made up of two parts. The port chamber is made up of a small reservoir and a septum that seals itself. The port chamber is usually made of metal or plastic and is placed under the skin on the upper chest. The catheter is a flexible tubing that connects to the port chamber. It is then threaded through a large vein and usually leads into the superior cava near the chest.

Power injection is the main purpose of PowerPort. It can, therefore, be used in procedures such as contrast-enhanced CT scanners, where rapid injection of contrast is needed. A special needle is used to access the port. It is inserted into the septum chamber of the port after being inserted under the skin. The port can be accesed by inserting a needle through the skin and into the septum of the chamber. This allows direct injections of medication or other fluids or blood into the bloodstream. The septum will re-seal itself after the needle has been removed.

Bard PowerPort: Patients express safety concerns

According to a review by Bard PowerPort of the complaints received from patients, the majority believe that the problem is the material used to make the catheter tubes. Many of these devices are made of polyurethane polymer, which is a flexible material created by mixing barium sulfate and polyurethane. There may be a problem with the high barium concentrations used by the company. This could lead to small cracks forming in the catheter tubing as well as other issues, such as the degradation of structural integrity.

Bard PowerPort products have also been reported to increase the risk of infection. The reason for this is that after the needle has been removed, it leaves behind a small opening that allows bacteria to grow.

What are the risks of a potentially defective Bard PowerPort?

Bard PowerPort has been linked to a variety of complications. These concerns are mainly related to blood clots and device movement from the original position. Infections and device failure are also common. These complications can cause any of the following symptoms:

• Blood Clots
• Cardiac arrhythmia,
• Cardiac arrhythmia,
• Cardiac Punctures,
• Cardiac/pericardial tamponade,
• Deep Vein Thrombosis (DVT),
• Hematomas,
• Hemorrhaging or Bleeding Injury
• Perforations in tissues, organs and vessels
• Pulmonary embolism
• Pain that is severe and persistent
• Blood vessels are torn apart.
• Infections.

There is a high risk of infection when doctors break the skin to insert an object or foreign body into the body. Bard powerport infections, however, tend to occur after the procedure. This means that the infection is less likely to be caused by the initial exposure and could instead be due to an issue with the Bard design.

Is There a Bard PowerPort recall?

The FDA issued a class 2 device recall for certain Bard PowerPort devices in 2020. However, in 2022, the FDA ended the recall after the company implemented corrective measures. According to the recent concerns expressed by many patients, there hasn’t been a Bard PowerPort Recall. Talking to an experienced Product Liability Lawyer can make you more informed about the topic.

Did the manufacturer know about problems with the Bard Power Ports?

It is unclear whether Bard was aware of any issues with the Bard’s power. In the Bard PowerPort suits, however, some patients claim that Bard knew that the device had a higher rate of failure and complications than other devices. The patients say that Bard should have issued clearer warnings regarding the risks associated with using the PowerPort.

Does there currently exist a Bard PowerPort Lawsuit?

Many patients claim they have suffered serious health effects from using a defective Bard PowerPort product. In August 2023, federal judges decided that all Bard PowerPort class actions filed in federal courts should be consolidated into an MDL lawsuit and heard by one judge. Anyone with the Catheter defects can hire an Bard PowerPort Attorney and can file the case.

What compensation may be available to patients through a Bard PowerPort Lawsuit?

The amount of damages awarded in a product-liability lawsuit depends on the environment and circumstances of the case, such as the severity and extent of the injuries suffered by the victim. As a rule, victims can receive compensation for both economic and non-economic damages if they successfully file a lawsuit. Economic damages, for example, include all past medical costs related to the patient’s injury as well as future medical expenses for follow-up treatment. Compensation may be available for the patient’s loss of wages or their reduced earning capacity.

In contrast, non-economic damages are meant to compensate victims of their injuries for the psychological and emotional impact their unwanted damage have had on their lives. Damages for emotional distress, pain and suffering and damage to family relationships are included.

CAN YOU FILE A BARD POWERPORT LAWSUIT?

You could be eligible to file a Bard PowerPort lawsuit if you have had the catheter port device for any medical use or procedure. The Justice Now is currently hearing from people who suffered complications after having a Bard PowerPort device implanted. However, we can also help people who have not yet been injured by the PowerPort device but have been instructed by their medical providers to have it removed before harm is done.