Injury guide

Port catheter problems

Updated Oct 6, 202626 sources

An implanted port is a small device under the skin with a tube into a large vein. Here is how infections, clots and tube problems are found, and what the port lawsuits claim.

What the public record says

These are cited sources. Their inclusion does not imply that they endorse People’s Justice or reviewed this page.

The evidence and its limits

Centers for Disease Control and Prevention · 2025

CLABSI Basics

Design:
Agency review
Participants:
Not a study: CDC guidance about all central lines, including implanted ports.
Finding:
Central lines, including ports, are much more likely than regular IVs to be a source of serious infection.
Main limitation
This is general guidance for all central lines. It does not compare port brands and cannot show that any one port caused an infection.

Read the source: CLABSI Basics (opens in a new tab) · Checked Oct 5, 2026

The short answer

What is an implanted port, and what can go wrong with it?
A port is a small device placed under the skin, most often in the chest. A thin tube runs from it into a large vein near the heart. The lawsuits focus on infection, blood clots, and tubes that break or move. [1]
What are the signs of port catheter problems, and when should I see a doctor?
MedlinePlus says to call your care team right away if the port seems to have moved. Also call if the site looks infected or you have a fever. The Bard and AngioDynamics case pages list the signs in more detail. [2]
How do doctors diagnose port catheter problems?
To look for infection, doctors test blood samples for germs. This test is called a blood culture. To look for a clot, a common test is an ultrasound of the vein. Scans can also show the tube itself. [3]
Which records show port catheter problems?
Lab reports give blood culture results and name any germ found. Scan reports describe a clot, a break or a tube that moved. A port’s label usually has a code, called a UDI, that names the exact model. [4]

What rules a case out

Not covered by this case

  • This page is not medical advice. Talk to your care team about your own port.
  • It does not cover PICC lines or other central lines that are not implanted ports.

What is an implanted port, and what can go wrong with it?

A port is a small device placed under the skin, most often in the chest. A thin tube runs from it into a large vein near the heart. The lawsuits focus on infection, blood clots, and tubes that break or move.

Ports are used when someone needs treatment for a long time, such as chemotherapy or antibiotics. A needle goes through the skin into the port’s silicone top. A port can stay in for weeks, months or years.

CDC counts a port as a central line, because its tube reaches a major vein close to the heart. CDC says central lines are much more likely than a regular IV to be a source of serious infection.

What are the signs of port catheter problems, and when should I see a doctor?

MedlinePlus says to call your care team right away if the port seems to have moved. Also call if the site looks infected or you have a fever. The Bard and AngioDynamics case pages list the signs in more detail.

A clot in an arm vein can cause swelling, redness and pain. NHLBI says these clots can form when a large central line sits in the vein, and that some cause no signs at all.

With a bloodstream infection, CDC says people may have a fever and red, sore skin around the line. If something seems wrong, tell the team that cares for your port. Bring a list of your questions to the visit.

How do doctors diagnose port catheter problems?

To look for infection, doctors test blood samples for germs. This test is called a blood culture. To look for a clot, a common test is an ultrasound of the vein. Scans can also show the tube itself.

A blood culture can show which germ is causing an infection, which helps doctors pick a treatment. Several cultures may be drawn. Some positive results come from germs on the skin, not a true infection.

Court papers in the Bard cases explain that Bard ports contain barium sulfate, which makes them show up on X-ray, CT and MRI scans.

Which records show port catheter problems?

Lab reports give blood culture results and name any germ found. Scan reports describe a clot, a break or a tube that moved. A port’s label usually has a code, called a UDI, that names the exact model.

To learn your exact port model, ask the hospital where it was placed for the record from that day. You can also search a brand name, such as PowerPort, BioFlo, Smart Port or Vortex, in AccessGUDID, a public FDA and National Library of Medicine database.

Federal privacy rules give you a right to copies of your own health records, including X-rays and other images.

What does research say about Bard and AngioDynamics ports and these problems?

Health agencies say any port can raise the risk of infection and clots, because its tube sits in a large vein. We found no FDA statement that links Bard or AngioDynamics ports to these problems.

FDA lists a few recalls of certain lots of both companies’ ports, for problems such as a wrong part, packaging that may not be sterile, or missing instructions. The recall records we read were not about the tube wearing down, infection or clots.

In the Bard cases, the judge has ruled on which expert opinions a jury may hear. In March 2026 the judge barred one expert from saying that the amount of barium sulfate in Bard ports raises the risk of clots and infection. Between March and September 2026, in three test cases, the judge turned down all or most of Bard’s requests to end the case before a trial.

Rulings like these decide what evidence may be used and whether a case can reach a jury. They are not findings that a port caused anyone’s harm. In the federal court records we read, we found no ruling that either company’s ports cause these problems.

In the AngioDynamics cases, the court set its schedule for shared expert questions to run into 2027.

Who brings port catheter claims in the Bard and AngioDynamics cases?

People who had a Bard or AngioDynamics port and later had an infection, a clot, or a tube that broke or moved brought these federal cases. They say too much barium sulfate weakened the tube. Your own records and facts decide whether you could bring a claim.

Each company’s cases are grouped in a different federal court. The Bard and AngioDynamics case pages explain what is happening in each one now.

Can a family member get records for someone with a port problem?

Yes, when the law gives them that role. Ports are often used for treatments such as chemotherapy, and a relative may want to help. A health care power of attorney lets an adult name someone to make health care decisions and get related records for them.

Parents can usually get the records of a child who has a port, with a few exceptions. After a death, the executor or administrator of the estate can get the records the estate needs. A care team may also tell a relative who helped with care about matters tied to that help, unless the person had said not to. State law fills in the details.

If someone died, the wrongful death case page explains in general how those claims work.

Sources

  1. NCI Dictionary of Cancer Terms: port
  2. MedlinePlus: Central venous catheters, ports
  3. MedlinePlus: Blood culture
  4. FDA: UDI basics
  5. CDC: Central line-associated bloodstream infection basics
  6. JPML transfer order, Bard port MDL No. 3081 (Aug. 8, 2023)
  7. JPML transfer order, AngioDynamics port MDL No. 3125 (Oct. 3, 2024)JPML transfer order, AngioDynamics port MDL No. 3125 (Oct. 3, 2024) · court
  8. NHLBI: Venous thromboembolismNHLBI: Venous thromboembolism · regulator
  9. MedlinePlus: Deep vein thrombosisMedlinePlus: Deep vein thrombosis · regulator
  10. MedlinePlus: Talking with your doctorMedlinePlus: Talking with your doctor · regulator
  11. D. Ariz.: Bard port MDL order on infection experts (Dec. 2025)D. Ariz.: Bard port MDL order on infection experts (Dec. 2025) · court
  12. AccessGUDID: PowerPort device recordsAccessGUDID: PowerPort device records · regulator
  13. AccessGUDID: AngioDynamics port device recordsAccessGUDID: AngioDynamics port device records · regulator
  14. HHS: Your right to access your health informationHHS: Your right to access your health information · regulator
  15. FDA recall Z-1570-2020: PowerPort implantable portFDA recall Z-1570-2020: PowerPort implantable port · regulator
  16. FDA recall Z-0076-2019: BioFlo portFDA recall Z-0076-2019: BioFlo port · regulator
  17. FDA recall Z-1466-2021: Smart Port CTFDA recall Z-1466-2021: Smart Port CT · regulator
  18. FDA recall Z-0132-2023: Vortex MP portFDA recall Z-0132-2023: Vortex MP port · regulator
  19. D. Ariz.: Bard port MDL order on a biomaterials expert (Mar. 30, 2026)D. Ariz.: Bard port MDL order on a biomaterials expert (Mar. 30, 2026) · court
  20. D. Ariz.: Bard port MDL order in an infection case (Mar. 5, 2026)D. Ariz.: Bard port MDL order in an infection case (Mar. 5, 2026) · court
  21. D. Ariz.: Bard port MDL order in a broken-catheter case (July 22, 2026)D. Ariz.: Bard port MDL order in a broken-catheter case (July 22, 2026) · court
  22. D. Ariz.: Bard port MDL order in a bloodstream infection case (Sept. 25, 2026)D. Ariz.: Bard port MDL order in a bloodstream infection case (Sept. 25, 2026) · court
  23. S.D. Cal.: AngioDynamics port MDL Case Management Order No. 7 (Oct. 31, 2025)S.D. Cal.: AngioDynamics port MDL Case Management Order No. 7 (Oct. 31, 2025) · court
  24. HHS: Personal representatives under HIPAAHHS: Personal representatives under HIPAA · regulator
  25. HHS: Health information of deceased individualsHHS: Health information of deceased individuals · regulator
  26. eCFR: 45 CFR 164.502(g), personal representativeseCFR: 45 CFR 164.502(g), personal representatives · regulator

Checked against 26 primary sources by People's Justice editors · Updated

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