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

Take action

Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Vascular Solutions is recalling Langston Dual Lumen Catheter model 5550 with certain lot numbers because the inner lumen may separate from the hub during pressure injection. This could lead to injury if the catheter is used incorrectly.

Why it’s dangerous

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

Who’s affected

Healthcare professionals using the Langston Dual Lumen Catheter model 5550 with specific lot numbers are most at risk. Patients receiving this catheter during medical procedures may also be affected.

How to tell if you have this one

Check the model number (5550) and lot numbers listed: 637973, 640204, 659555, 660597, 633668, 663767, 669593, 659856, 644096, 676528, 672481, 632704, 656792, 658273, 666755, 635885.

Brand
Vascular Solutions
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the model number (5550) and lot numbers listed in the recall notice.
Stop Using if Suspect
If you have the recalled model with a listed lot number, stop using it immediately to prevent potential injury.

✎ GovInfoNow

Questions people ask

What is the specific model number of the recalled catheter?

The specific model number is 5550.

Which lot numbers are affected?

Affected lot numbers include 637973, 640204, 659555, 660597, 633668, 663767, 669593, 659856, 644096, 676528, 672481, 632704, 656792, 658273, 666755, and 635885.

Is there a fix for this issue?

The recall notice does not mention a fix or remedy for this issue.

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-0113-2021 — Vascular Solutions Vascular Solutions

Hello,

I own a Vascular Solutions that is covered by recall Z-0113-2021 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0113-2021 (August 31, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0113-2021 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.

Use caution until it’s fixed