# FDA recall Z-2745-2026

> **Terex Utilities** · Class II · device recall initiated 2026-05-11.

## Product

Power Over Fiber Base Module

## Reason for 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

## Distribution

U.S. Nationwide Distribution and International Distribution

## Key facts

- **Recall number:** Z-2745-2026
- **Recalling firm:** Terex Utilities
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-11
- **Report date:** 2026-08-05

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Watertown, SD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2745-2026

## Citation

> AI Analytics. FDA recall Z-2745-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2745-2026. Source: US FDA. Licensed CC0.

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