Terex Utilities recalls Power Over Fiber Base Module
- 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.