The FDA has received numerous reports of severe adverse incidents associated with the implantable Bard PowerPort catheter. These incidents encompass device fractures and infections, which carry the potential risk of causing heart attacks, strokes, hemorrhages, blood clots, sepsis, necrosis, and other life-threatening events. Patients have reported various complications including catheter malfunctions, infections, port migration, thrombosis, and breakage, all of which have prompted the recall by Bard, the manufacturer. If you experienced serious injury after receiving an implantable Bard PowerPort catheter, you may be eligible for compensation. Call Attorney Marilyn McGoldrick at 888-491-9726 to discuss your legal rights.

What is a Bard PowerPort?

A Bard Power Port, also known as a BardPort or Bard Power Injectable Port, is a medical device designed for the easy and convenient administration of medications, fluids, and other treatments into a patient’s bloodstream. It consists of a small implantable port placed beneath the skin, typically in the chest area, and a catheter that connects to a large vein. This device is commonly used in medical situations such as chemotherapy, long-term antibiotic therapy, and frequent blood draws, to minimize the need for repeated needle insertions.

Bard Power Port Recall

Concerns have arisen regarding the safety and reliability of Bard Power Ports, leading to a significant recall of these devices. In March of 2020, the FDA issued a Class 2 recall encompassing three specific models of the Bard PowerPort. The recall was initiated due to a range of concerns, including instances of bloodstream infections, device displacement, catheter breakage, and thrombosis.  Bard PowerPort devices are crafted from a material called Chronoflex, a pliable polymer containing barium. Elevated barium concentrations can lead to the deterioration of the polymer, potentially causing tube fractures, degradation, fissures, and cracks.

Bard products which may be linked to serious injury after device fracture or infections include:

  • Bard Power-Injectable Implantable Ports (PowerPorts®)
  • BardPort®, SlimPort®, And X-Port® Implanted Ports
  • Power-Injectable Implantable Ports With Chronoflex Polyurethane Catheters
  • PowerPort duo MRI Implantable Port
  • PowerPort Implantable Port
  • PowerPort ClearVUE Slim Implantable Port
  • PowerPort ClearVUE isp Implantable Port
  • PowerPort Duo MRI Implanted Port With 9.5 Fr. Dual Lumen Chronoflex Polyurethane Catheter
  • PowerPort Implanted Port With Groshong Catheter
  • PowerPort MRI Implanted Port With 9.6 Fr Silicone Catheter
  • Titanium PowerPort isp Implanted Port With 6 Fr Chronoflex Polyurethane Catheter
  • Titanium PowerPort isp Implanted Port

Injuries Linked to the Bard Power Port

Several injuries and complications have been linked to Bard Power Ports, prompting the recall and raising concerns among patients and healthcare providers. Some of the reported issues include:

  1. Catheter Malfunctions: Instances where the catheter becomes kinked or damaged, hindering the flow of fluids or medications into the bloodstream.
  2. Infections: Patients have experienced infections around the implant site or along the catheter, which can lead to severe health complications.
  3. Port Migration: The port can shift or move from its original placement, making it challenging to access and potentially causing injury to nearby tissues or vessels.
  4. Thrombosis: Blood clots forming around the port or catheter, which can obstruct the flow of blood and lead to serious medical conditions like deep vein thrombosis (DVT).
  5. Breakage: Rare instances of the port or catheter breaking, which can result in surgical intervention to remove the device.

These issues underscore the importance of addressing the Bard Power Port recall to prevent further harm to patients relying on these devices.

What Can You Do?

If you or a loved one has been affected by the Bard Power Port recall or experienced any complications related to this medical device, it is crucial to take the following steps:

  1. Consult with a Healthcare Professional: Reach out to your healthcare provider immediately if you suspect any issues with your Bard Power Port or experience symptoms of complications, such as pain, swelling, or signs of infection.
  2. Stay Informed: Stay updated on the latest developments regarding the Bard Power Port recall through official healthcare channels and announcements from Bard or regulatory authorities.
  3. Legal Consultation: Consider seeking legal advice if you believe you have suffered harm or injuries due to a Bard Power Port malfunction or related complications. An attorney experienced in medical device recalls can help you understand your rights and options. If you or a loved one was given an implanted Bard Power Port and suffered injuries as a result, please contact the Thornton Law Firm at 888-491-9726 to speak to attorney Marilyn McGoldrick about a potential case.

Ultimately, your health and well-being are paramount, and taking prompt action in response to the Bard Power Port recall is essential to ensuring your safety and getting the necessary medical support.