Published by If you have an implanted Bard Power Port device and experienced complications such as catheter fracture, infection, thrombosis or migration—you may be eligible for legal review and compensation.
Our legal team offers a free, no-obligation consultation and accepts representation on a contingency-fee basis.
Table Of Contents
What’s the Problem?
The Bard Power Port is an implantable vascular access port system used to provide long-term intravenous or medication delivery via a subcutaneous port and catheter. [1]
Lawsuits allege that the device includes design and manufacturing defects—particularly in the catheter tubing material (including barium sulfate-filled polyurethane blends) —that have made the catheter portion prone to fracture, migration and breakdown inside the body. [2]
When these defects occur, patients may require additional surgery, develop serious infections, thrombosis, embolism or other life-threatening complications. [3]
Latest Updates
- November 4, 2025 – The Bard PowerPort lawsuits have surpassed 2,000 pending claims in the federal multidistrict litigation (MDL No. 3081) in the U.S. District Court for Arizona. [1]
- October–November 2025 – Plaintiffs continue to file new claims alleging catheter fracture, migration and subsequent thrombosis or infections requiring surgery. [3]
- 2026 and beyond – Bellwether trials are scheduled to test evidence of defects and cause, paving the way for potential settlement negotiations. [4]
Product & Usage Overview
The Bard Power Port system consists of a titanium or stainless-steel port implanted beneath the skin, connected to a catheter inserted into a major vein. [5]
Typical uses include long-term chemotherapy, frequent IV medication administration, blood sampling, and nutrition support in patients with chronic conditions. [6]
Allegations in the lawsuits point to the catheter tubing material—specifically its incorporation of barium sulfate for radiopacity—which over time may cause cracks, micro-fractures and separation of material, leading to structural failure under in-vivo pressures.
Once a fracture or migration occurs, components can travel through the bloodstream, puncture vessels, cause occlusions, require surgical retrieval or lead to other severe complications.
Injuries & Side Effects
- Catheter fracture: Pieces of the catheter may break off, travel through the vascular system and block critical arteries or lodge in organs. [2]
- Migration: The port or catheter can move from its original placement, causing loss of function or damage to surrounding tissues and vessels. [3]
- Infection/sepsis: Cracks or degradation of catheter surfaces may allow bacteria to enter, resulting in difficult-to-treat bloodstream infections. [6]
- Thrombosis/embolism: Irregular surfaces or migrating fragments can promote clot formation that may travel to the lungs (pulmonary embolism) or heart. [4]
Do You Qualify for a Bard Power Port Lawsuit?
You may qualify if you:
- Had a Bard Power Port device implanted (including models like ClearVUE™, Slim, MRI-compatible ports) and subsequently experienced complications such as catheter fracture, migration, infection, or thrombosis.
- Suffered medical intervention, revision surgery, hospitalization or serious health damage connected to the device failure.
- Have medical records, device identification (implant date, model), proof of complication and documentation of additional care required.
- Are within your state’s statute of limitations for product liability or medical-device injury claims; timely consultation is critical.
Evidence You Should Gather
- Medical records showing the implant procedure, device model and date.
- Operative/surgical reports or interventional radiology records showing fracture retrieval, migration or malfunction.
- Imaging studies (X-ray, CT) showing device pieces, migration or vessel damage.
- Hospital bills, treatment records, medication logs, lost wage documentation.
- Any correspondence from healthcare provider, manufacturer or regulatory body about device problems or warnings.
Damages You Can Recover
Possible recoverable damages include:
- Medical expenses: Surgeries, hospital stays, follow-up treatments, medications.
- Lost wages: Time out of work, permanent disability or decreased earning capacity.
- Pain and suffering: Physical pain, emotional distress, long-term health impact.
- Device removal/replacement costs: Additional procedures, revision surgery and related care.
While the Bard Power Port litigation is active and no large-scale global settlement has been reported, law firms estimate some fracture-related claims could reach mid to high six-figure amounts depending on severity and medical consequence.
Legal Theories & Liability Grounds
Potential legal claims include:
- Defective product: The device was manufactured or designed with inherent flaws making it unreasonably dangerous for its intended use.
- Negligence: The manufacturer may have failed to test, design, inspect or warn about risks associated with the catheter materials or structure.
- Failure to warn: Allegations that the manufacturer did not adequately inform doctors, hospitals or patients about the risk of fracture, migration, infection or thrombosis.
- Strict product liability: The device entered commerce in a dangerous condition and caused harm regardless of negligence.
- Breach of warranty: The device was marketed for safe long-term vascular access yet allegedly did not meet that promise.
Statute of Limitations & Timing
Claims for medical-device injuries typically carry deadlines between one and three years depending on the jurisdiction and when the harm was discovered. Because Bard Power Port litigation is ongoing and bellwether trials are scheduled starting in 2026, acting promptly helps preserve evidence like implant records, imaging, device identifiers and care documentation.
Frequently Asked Questions
- Can I still file a case if my device caused an infection but no fracture?
Yes — if you had a Bard Power Port implant and experienced documented injuries such as serious infection or thrombosis, you may still qualify. - Is this a class-action lawsuit?
No — The Bard Power Port litigation is consolidated via a Multidistrict Litigation (MDL) rather than a traditional class action, allowing individual claims to proceed. [3] - What should I do if I still have the device implanted and no symptoms yet?
Keep your implant records, register your device if notified, maintain medical follow-up and consult an attorney if you begin experiencing complications.
Why You Should Act Now
The Bard Power Port lawsuit presents a serious opportunity for individuals harmed by what is alleged to be a defective vascular access device commonly used in chemotherapy, nutrition support and long-term IV therapy. If you have been implanted with one of these devices and experienced complications like fracture, migration, infection or clotting—consulting an experienced medical-device attorney today can preserve your rights, strengthen your position and increase your chances of compensation.
References
- https://www.lawsuit-information-center.com/bard-powerport-lawsuit.html
- https://www.wernerhoffman.com/mass-tort-lawyer/bard-powerport/
- https://www.torhoermanlaw.com/bard-powerport-lawsuit/
- https://www.lanierlawfirm.com/bard-powerport-lawsuit/
- https://www.sokolovelaw.com/product-liability/medical-devices/bard-powerport/
- https://www.dolmanlaw.com/product-liability-lawyer/bard-powerport/