Covidien Valleylab FT10 Energy Platform Software Error May Cause Inoperable System

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Contact the company & request your remedy

Recalling firmCovidien200 Medtronic Dr, N/A · Lafayette, CO 80026

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Covidien is recalling Valleylab FT10 Energy Platform systems with software versions 4.0.1 to 4.0.3. These systems may become inoperable due to a software error, preventing proper use.

Why it’s dangerous

The software error can cause the system to become inoperable, meaning it may not function properly. This could prevent the system from being used for its intended medical purpose, potentially interrupting patient care.

Who’s affected

Healthcare professionals using Valleylab FT10 Energy Platform systems with specific software versions are most at risk. Patients using these systems may experience interrupted care if the system becomes inoperable.

How to tell if you have this one

Check for the model references VLFT10GEN, DLVLFT10GEN, or VLFT10GENZD with software versions 4.0.1, 4.0.2, or 4.0.3. The product includes specific serial numbers listed in the recall notice.

Brand
Covidien
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify the software version on your Valleylab FT10 Energy Platform system. If it is 4.0.1, 4.0.2, or 4.0.3, it is affected.

✎ GovInfoNow

Questions people ask

What software versions are affected?

Software versions 4.0.1, 4.0.2, and 4.0.3 are affected.

How can I tell if my system is affected?

Check for the model references VLFT10GEN, DLVLFT10GEN, or VLFT10GENZD with software versions 4.0.1, 4.0.2, or 4.0.3.

What should I do if my system is affected?

The recall does not specify a remedy, so contact the manufacturer for guidance on next steps.

Take action

Contact Covidien

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

✉️ Open in email

Subject: Recall Z-0631-2024 — Covidien Covidien

Hello,

I own a Covidien that is covered by recall Z-0631-2024 from Covidien.

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-0631-2024 (November 16, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0631-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

Covidien recalls Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD

Lower-risk recall