DeviceSignal · Recall classified
Terex Utilities
FDA classified a device recall on 2026-07-30 · Class II · Z-2745-2026
EventRecall classified
Effective2026-07-30
ClassificationClass II
On 2026-07-30 the FDA classified a device recall from Terex Utilities as Class II. Product: Power Over Fiber Base Module. Recall Z-2745-2026. The firm initiated it on 2026-05-11. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2745-2026
- Classification
- Class II
- Classified on
- 2026-07-30
- Initiated on
- 2026-05-11
- Firm
- Terex Utilities
- Reason
- 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
- Product
- Power Over Fiber Base Module
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2745-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
43214ab044a39e99501322f4a44488041a8c44838cf17001200fae988db1fb85- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)