IPG Medical Thuvera Laser Console Software 2.2 Recall: False Error Code 5018 Display

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Contact the company & request your remedy

Recalling firmIPG Medical Corporation225 Cedar Hill St, N/A · Marlborough, MA 01752-5900

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

IPG Medical is recalling Thuvera Laser Console software version 2.2 for a false error code 5018 display. This issue does not cause safety risks or injuries, so no action is required.

Why it’s dangerous

The software anomaly causes the device to display error code 5018 incorrectly, which might lead to confusion about the device's status. However, this does not cause physical harm or safety issues.

Who’s affected

Users of Thuvera Laser Console software version 2.2 (model MD2300F-001507) who have the listed serial numbers. Medical professionals using this device are most at risk if they misinterpret the error code.

How to tell if you have this one

Check if your Thuvera Laser Console has software version 2.2 (model MD2300F-001507) and one of the listed serial numbers. The device may show error code 5018 falsely.

Brand
IPG Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify your Thuvera Laser Console software version is 2.2 (model MD2300F-001507) by checking the device settings or documentation.

✎ GovInfoNow

Questions people ask

Do I need to do anything with this device?

No action is needed as the false error code 5018 display does not pose a safety risk.

What if I see error code 5018?

This is a false display caused by software version 2.2; it does not indicate a real problem with the device.

Is this recall dangerous?

No, the recall is for a software display issue that does not cause injuries or safety hazards.

Take action

Contact IPG Medical

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

✉️ Open in email

Subject: Recall Z-2554-2026 — IPG Medical IPG Medical

Hello,

I own a IPG Medical that is covered by recall Z-2554-2026 from IPG Medical.

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-2554-2026 (May 5, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2554-2026 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.

IPG Medical Corporation recalls Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

Lower-risk recall