Lower risk Medical device recall · FDA · Published May 11, 2026

Terex Power Over Fiber Base Module Recall: Incorrect Laser Class Labeling

Terex Utilities recalls Power Over Fiber Base Modules with incorrect laser class labeling. Products may not be certified for safety, risking injury from improper laser exposure. Affected units include specific part numbers.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2745-2026Medical device Terex Utilities ›

Lower-risk recall

Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for device. Improperly labeled - omitted labels required under 21 CFR 1040.10 / IEC 60825-1 via LN#56. Missing certification and proper manufacturer's ID label. Was not accompanied by compliant User Information. Formalized quality control procedures and record keeping of QC testing was not performed to IEC 60825-1 nor 21 CFR 1040.10 standards. Sales information did not convey required class designation and warning statement

✎ GovInfoNow plain-language explainer

Terex Utilities is recalling Power Over Fiber Base Modules due to incorrect laser class labeling and missing safety certifications. This could lead to unsafe laser exposure if the device is used without proper certification. Read more at govinfonow.com/recall/169462-terex-power-over-fiber-base-module-recall-incorrect-laser-class.

Source Summary by GovInfoNow · govinfonow.com/recall/169462-terex-power-over-fiber-base-module-recall-incorrect-laser-class · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2745-2026

Cite this page

“Terex Power Over Fiber Base Module Recall: Incorrect Laser Class Labeling.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/169462-terex-power-over-fiber-base-module-recall-incorrect-laser-class. Based on FDA recall #Z-2745-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2745-2026%22&limit=1).

The FDA announced on May 11, 2026, that Terex Utilities is recalling Power Over Fiber Base Modules because they lack required laser safety certifications and proper labeling. The agency mandates the recall of these devices distributed nationwide and internationally.

How to tell if you have it

Brand: Terex Utilities
Product: Power Over Fiber Base Module
Part Numbers: P/N 633232, P/N 622365, P/N 633383, P/N 633910, P/N 635731
Quantity: 101 units

The hazard

The devices were distributed without a laser product report filed with the CDRH and incorrectly labeled as Class IV instead of Class 1. They also omitted required labels under 21 CFR 1040.10 / IEC 60825-1, lacked manufacturer ID labels, and were not accompanied by compliant User Information.

Context

GovInfoNow's records show other recent recalls of similar products include the Repligen Maverick Measurement Module Spectrometer Recall (2025-12-10), the Beaver-Visitec OME6000U Laser System Recall (2025-12-05), and the Lutronic DermaV Laser System Recall (2026-08-06).

How to tell if you have this one

Check for part numbers 633232, 622365, 633383, 633910, or 635731 on the device. The product was sold without proper safety labels and certifications required by U.S. and international standards.

Brand
Terex Utilities
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Labels
Look for the part numbers 633232, 622365, 633383, 633910, or 635731 on the device.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “U.S. Nationwide Distribution and International Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 3 months after the firm started it.

May 11, 2026Firm started the recall
Jul 30, 2026FDA classified it Class II
Aug 5, 2026Published in FDA’s Enforcement Report
Aug 11, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/169462-terex-power-over-fiber-base-module-recall-incorrect-laser-class">Terex Power Over Fiber Base Module Recall: Incorrect Laser Class Labeling (GovInfoNow)</a>

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-2745-2026 (May 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2745-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.