{"recall":{"id":"fda-device-99382","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Terex Utilities recalls Power Over Fiber Base Module","firm":"Terex Utilities","date":"2026-05-11","reported":"2026-08-05","status":"Ongoing","classification":"Class II","products":[{"name":"Power Over Fiber Base Module","code":"Power Over Fiber Base Module Identification P/N 633232 P/N 622365 P/N 633383 P/N 633910 P/N 635731","quantity":"101","number":"Z-2745-2026","classification":"Class II"}],"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","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"U.S. Nationwide Distribution and International Distribution","nationwide":true,"states":[],"units":"101","remedy":"","whatToDo":"Check your product against the names and codes above. The FDA enforcement record lists the recall as fda mandated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.","contact":"","url":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99382","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"8f1ae5b7cb2968cf","firstSeen":"2026-11-02T13:57:14.206Z","updatedAt":"2026-11-02T13:57:14.206Z","history":[]},"official":{"fetchedAt":"2026-11-02T13:57:14.206Z","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","officialUrl":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99382","record":[{"status":"Ongoing","city":"Watertown","state":"SD","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99382","recalling_firm":"Terex Utilities","address_1":"600 Oakwood Rd","address_2":"N/A","postal_code":"57201-4140","voluntary_mandated":"FDA Mandated","initial_firm_notification":"Letter","distribution_pattern":"U.S. Nationwide Distribution and International Distribution","recall_number":"Z-2745-2026","product_description":"Power Over Fiber Base Module","product_quantity":"101","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_initiation_date":"20260511","center_classification_date":"20260730","report_date":"20260805","code_info":"Power Over Fiber Base Module Identification P/N 633232  P/N 622365 P/N 633383 P/N 633910  P/N 635731"}]}}