LeMaitre Chevalier Valvulotome Recall: Burrs May Tear Veins

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Contact the company & request your remedy

Recalling firmLeMaitre Vascular, Inc.32 3rd Ave, N/A · Burlington, MA 01803-4414

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

LeMaitre Vascular is recalling Chevalier Valvulotomes that may have burrs causing veins to tear during surgery. This is a serious risk for patients undergoing vein graft procedures.

Why it’s dangerous

Burrs (molding flash) on the cutter tip can tear the harvested vein during surgery. This could lead to serious complications like bleeding or infection in patients needing vein grafts.

Who’s affected

Surgical teams using Chevalier Valvulotomes for vein graft procedures are affected. Patients undergoing vein graft surgeries are at risk of vein tearing.

How to tell if you have this one

Check for Chevalier Valvulotomes with Catalog numbers 40025, 40030, or 40035. Lot numbers start with CHV (e.g., CHV1001, CHV1002, etc.).

Brand
LeMaitre Vascular
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop using it now
Immediately stop using the Chevalier Valvulotome if it has a lot number starting with CHV.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The Chevalier Valvulotome may have burrs that can tear the harvested vein during surgery.

Which models are affected?

Catalog numbers 40025, 40030, and 40035 with lot numbers starting with CHV (e.g., CHV1001, CHV1002).

Is there a fix for this issue?

The recall does not specify a remedy; affected units should be stopped use immediately.

Take action

Contact LeMaitre Vascular

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

✉️ Open in email

Subject: Recall Z-2468-2023 — LeMaitre Vascular LeMaitre Vascular

Hello,

I own a LeMaitre Vascular that is covered by recall Z-2468-2023 from LeMaitre Vascular.

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-2468-2023 (July 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2468-2023 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.

LeMaitre Vascular, Inc. recalls The Chevalier Valvulotome is a device used to disrupt the valves of veins which are to be used as grafts in the in situ

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