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CLASS II · ModerateFDA

Terex Utilities recalls Power Over Fiber Base Module

📅 May 11, 2026 · 📍 Nationwide
Recalling company
Terex Utilities
Product
Power Over Fiber Base Module
Reason
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
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
May 11, 2026
Reported
Aug 5, 2026
Distribution
U.S. Nationwide Distribution and International Distribution
Status
Ongoing
Quantity
101
Lot / codes
Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731
Company location
Watertown, SD
Recall type
FDA Mandated
Recall number
Z-2745-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2745-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.