Terex Utilities: Power Over Fiber Base Module
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Terex Utilities
- Product
- Power Over Fiber Base Module
- Reason / 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
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- U.S. Nationwide Distribution and International Distribution
- Recall initiated
- 2026-05-11
- Code info
- Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731
- Product quantity
- 101
- Voluntary mandated
- FDA Mandated
- City
- Watertown
- State
- SD
- Country
- United States
- Event id
- 99382
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