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FDA · Medical devices ·

Power Over Fiber Base Module recall

Terex Utilities recalled Power Over Fiber Base Module on August 5, 2026 because of device not certified - no laser product report was filed with CDRH prior to distribution. It was sold nationwide.

Why it was recalled

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…

What's recalled

Power Over Fiber Base Module

Quantity: 101

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice