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Terex Utilities recalls Power Over Fiber Base Module

Recalled August 5, 2026 · FDA recall Z-2745-2026 · Terex Utilities

Hazard
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 · FDA Class II
Units
101
Sold at
U.S. Nationwide Distribution and International Distribution

Description

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

Product
Power Over Fiber Base Module
Manufacturer(s)
Terex Utilities

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →

Terex Utilities recalls Power Over Fiber Base Module | RecallWatchUSA