FDAClass II · Medical device · Recall Z-2745-2026 · Recalled August 5, 2026

Power Over Fiber Base Module recall — Terex Utilities

Agency report date: August 5, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Power Over Fiber Base Module
Company / brand: Terex Utilities
Lot / serial / date codes: Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731
Distribution: U.S. Nationwide Distribution and International Distribution

Agency product description and boundaries

Power Over Fiber Base Module

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Power Over Fiber Base Module

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2745-2026
Brand: Terex Utilities
Classification: Class II
Units affected: 101
Recall status: Ongoing
Initiated: FDA Mandated

Affected products

Power Over Fiber Base Module

Companies & origin

Recalling firm location: Watertown, SD, United States
Firm address: 600 Oakwood Rd, N/A, 57201-4140

Identifying details (verbatim from the notice)

Product codes / lots: Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731
Distribution: U.S. Nationwide Distribution and International Distribution
Firm notified the public via: Letter
FDA event ID: 99382
Recall initiated: May 11, 2026
FDA classified: July 30, 2026
FDA report date: August 5, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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