What Should I Do If I Experienced Complications with a Bard PowerPort Implant?

About Bard PowerPort cases

The Bard PowerPort is a type of implanted medical device used to provide easy access to veins for patients who need frequent injections, blood draws, or intravenous treatments. While these devices are commonly used in hospitals and clinics, there have been reports of serious complications, including device fractures, infections, and blood clots (thrombus formation).

Some patients with Bard PowerPort implants have experienced pain, swelling, or other symptoms that may be related to device malfunction or failure. In response, lawsuits have been filed alleging that certain Bard PowerPort models may be prone to breaking, leaking, or causing injury inside the body. These lawsuits are currently being coordinated as part of a federal multidistrict litigation (MDL 3081).

If you or a loved one has suffered complications after receiving a Bard PowerPort, you may be wondering about your legal options. This page explains common issues reported with Bard PowerPort devices and outlines how you can connect with law firms reviewing potential claims.

Who may qualify for review

Law firms reviewing Bard PowerPort cases typically look for certain factors when considering potential claims. These may include whether you had a Bard PowerPort device implanted, the type of complications you experienced (such as device fracture, infection, blood clots, or the need for additional surgeries), and the timing of your symptoms relative to your device placement. Medical records showing the type of device used, the date of implantation, and any follow-up treatments or hospitalizations can be helpful for a legal review. If your Bard PowerPort was removed, replaced, or examined due to complications, documentation of these events may also be important. Other factors that might be considered include your overall health history, the specific Bard PowerPort model involved, and whether you received warnings or information about possible device risks. Each case is unique, and eligibility for legal action depends on the facts and applicable state law. Participating law firms may offer a free review of your situation to help determine whether your circumstances fit the criteria for ongoing lawsuits. Submitting your information does not guarantee that a law firm will take your case or that you will be eligible for compensation.

Information that may help

You do not need every record before starting, but these details help a participating law firm understand your situation faster.

• Medical records showing Bard PowerPort implantation, including date and facility
• Device identification card or documentation with model and serial number
• Records of any complications, such as infection, device fracture, or blood clots
• Hospital or surgical reports related to Bard PowerPort removal or revision
• Imaging studies (X-rays, CT scans, ultrasounds) showing device condition or complications
• Physician notes describing symptoms or adverse events linked to the device
• Pharmacy records for antibiotics or other treatments related to device complications
• Photographs of visible injuries, scars, or device site reactions (if available)
• Correspondence with healthcare providers about device issues or recommendations
• Discharge summaries or after-visit instructions mentioning Bard PowerPort problems
• Any recall or safety notice received about the Bard PowerPort device

Deadline note

Deadlines for taking legal action, often called statutes of limitations, vary by state and can depend on the specific facts of your case, such as when you first noticed complications or when the device was implanted. Because waiting too long could affect your ability to pursue a claim, it is important to speak with a qualified attorney as soon as possible to understand your options and protect your rights.

Questions people ask about Bard PowerPort