Recall
FDAHealthMay 11, 2026

Terex Utilities — Power Over Fiber Base Module

⚠️ 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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 11, 2026

U.S. Nationwide Distribution and International Distribution

What's affected?

Product
Power Over Fiber Base Module
Lot code
Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731

Additional details

Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731

What should I do?

Recommended action

Class II recall. FDA Mandated Quantity affected: 101.

View original FDA notice →

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