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Langston V2 Catheter Recalled for Patient Injury Risk

Langston V2 Catheter Recalled for Patient Injury Risk

July 7, 2014 — Vascular Solutions, Inc., is voluntarily recalling a catheter that is used to deliver dye in imaging tests.

The problem is that the inner catheter can separate from the device hub during use. If this problem occurs, patients will require an intervention procedure to retrieve the broken device from their bloodstream. If it travels in the bloodstream, it could cause life-threatening adverse health consequences, including death.

The recall affects about 8,500 Langston V2 Dual Lumen Pressure Monitoring Catheters that were manufactured between January and April and sold until May. About 86% of inventory has been accounted for, and Vascular Solutions has notified customers by letter and phone about the recall.

The catheter is used to deliver dye (contrast medium) into a patient’s blood vessels during medical imaging tests (angiographic studies) that allow clinicians to see internal body structures. The device also measures pressure within the blood vessel.


  • Remove affected devices and place them in a secure area.
  • Complete and return the “VSI Account Inventory Form” included with the letter.
  • Returned devices will be replaced by Vascular Solutions.

The recalled catheters can be identified by looking up a list of affected lot numbers.

Do I have a Catheter Injury Lawsuit?

The Schmidt Firm, PLLC is currently accepting catheter induced injury cases in all 50 states. If you or somebody you know has been injured by the Langston V2 Dual Lumen Pressure Monitoring Catheter, you should contact our lawyers immediately for a free case consultation. Please use the form below to contact our Defective Medical Device Litigation Group or call toll free 24 hours a day at (866) 920-0753.

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