Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Langston Dual Lumen Catheter 6F Model 5540. For delivery of Recalled by Vascular Solutions, Inc. Due to The inner lumen of the Langston catheter may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Vascular Solutions, Inc. directly.
Affected Products
Langston Dual Lumen Catheter 6F Model 5540. For delivery of contrast medium in angiographic studies
Quantity: 30,877 units
Why Was This Recalled?
The inner lumen of the Langston catheter may separate from the hub during pressure injection.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Vascular Solutions, Inc.
Vascular Solutions, Inc. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report