Terex Utilities Power Over Fiber Base Module Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Terex Utilities is recalling 101 Power Over Fiber Base Modules due to missing certification, improper labeling, and lack of required user information.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Terex Utilities is conducting an FDA-mandated recall of the Power Over Fiber Base Module because the device was distributed without a laser product report filed with CDRH. The product label incorrectly states it is "Class IV" when Class 1 is appropriate, required labels under 21 CFR 1040.10 and IEC 60825-1 are omitted, and it lacks compliant user information. Formalized quality control procedures were not performed.
Which Products Are Affected
The recall involves the Power Over Fiber Base Module with identification numbers P/N 633232, P/N 622365, P/N 633383, P/N 633910, and P/N 635731. A total of 101 units were distributed nationwide in the United States and internationally. The recall number is Z-2745-2026.
What You Should Do
Consumers should contact Terex Utilities regarding the recalled devices.
Why This Matters
The recall addresses certification, labeling, and documentation deficiencies for a laser-related device distributed across the U.S. and internationally.
Source
FDA recall Z-2745-2026. https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,063 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.