Power Over Fiber Base Module
Published August 5, 2026 · Recall initiated: May 11, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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
What to do
FDA Mandated · Letter
Recall details
- Manufacturer
- Terex Utilities
- Distributor
- U.S. Nationwide Distribution and International Distribution
- Lot
- Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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