FDA Devices recall · Reported August 5, 2026
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 f…
Terex Utilities recalled Power Over Fiber Base Module - a moderate-severity action.
Power Over Fiber Base Module was recalled by Terex Utilities in August 5, 2026. Reason: Device not certified - no laser product report was filed with CDRH prior to distribution. Product label inco…. Check the official notice for the remedy. Verify recall #Z-2745-2026 with the FDA Devices before acting.
The recall
Terex Utilities issued this moderate-severity FDA Devices recall-Device not certified - no laser product report was filed with CDRH prior to distribution. Product label inco….
- Moderate
- severity level
- 101 units
- affected scope
- Class II
- classification
- August 5, 2026
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2745-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2745-2026) was formally reported on August 5, 2026, with the manufacturer initiating the action on May 11, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Terex Utilities is listed as the recalling firm, operating out of Watertown, SD. Federal records list the affected scope as 101.
The documented reason for this recall is: 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… Distribution data in the federal record shows the product reached: U.S. Nationwide Distribution and International Distribution. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 41,021 medical devices recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
Power Over Fiber Base Module
Reason for recall
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
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2745-2026 |
| Date reported | August 5, 2026 |
| Date initiated | May 11, 2026 |
| Recalling firm | Terex Utilities |
| Firm location | Watertown, SD |
| Affected scope | 101 |
| Distribution | U.S. Nationwide Distribution and International Distribution |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2745-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026