Vascular Solutions Langston Dual Lumen Catheter Recall: Inner Lumen May Separate During Injection

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Contact the company & request your remedy

Recalling firmVascular Solutions, Inc.6420 Sycamore Ln N, N/A · Maple Grove, MN 55369-6013

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Vascular Solutions is recalling Langston Dual Lumen Catheters with certain model and lot numbers because the inner lumen can separate from the hub during pressure injection. This could lead to complications during medical procedures if the catheter is used.

Why it’s dangerous

The inner lumen of the catheter may separate from the hub when pressure is applied during injection. This separation could cause the catheter to malfunction or become dislodged during medical procedures, potentially leading to complications.

Who’s affected

Healthcare professionals using the Langston Dual Lumen Catheter for medical procedures are most at risk. Patients receiving these catheters during treatment may also be affected.

How to tell if you have this one

Check the model number on the catheter, which is 5515. Look for lot numbers: 635806, 640206, 644140, 648701, 654143, 658252, 659635, 661470, 665301, 670376, 654130, 672728, 656020, 638111, or 677058.

Brand
Vascular Solutions
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Number
Verify the model number is 5515 to confirm if the catheter is affected.
Contact Manufacturer
Reach out to Vascular Solutions for further assistance if you have the affected model and lot numbers.

✎ GovInfoNow

Questions people ask

What is the specific model number of the recalled catheter?

The model number is 5515.

Which lot numbers are affected?

Lot numbers 635806, 640206, 644140, 648701, 654143, 658252, 659635, 661470, 665301, 670376, 654130, 672728, 656020, 638111, and 677058 are affected.

Is there a remedy for the recalled catheters?

The recall record does not specify a remedy.

Take action

Contact Vascular Solutions

We’ve drafted a message you can send Vascular Solutions to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0110-2021 — Vascular Solutions Vascular Solutions

Hello,

I own a Vascular Solutions that is covered by recall Z-0110-2021 from Vascular Solutions.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0110-2021 (August 31, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0110-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Vascular Solutions, Inc. recalls Langston Dual Lumen Catheter

Lower-risk recall