{"recall":{"id":"fda-device-99631","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Spectral Instruments Inc recalls 2 products","firm":"Spectral Instruments Inc","date":"2026-07-24","reported":"2026-08-26","status":"Ongoing","classification":"Class II","products":[{"name":"Lago X","code":"All serial numbers.","quantity":"40","number":"Z-2939-2026","classification":"Class II"},{"name":"Ami HTX","code":"All serial numbers.","quantity":"35","number":"Z-2940-2026","classification":"Class II"}],"reason":"Momentary absence of On-Screen \"X-Ray On\" banner during run readiness check.","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"United States.","nationwide":false,"states":[],"units":"40; 35","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=99631","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"cc474caa8f330a68","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=99631","record":[{"status":"Ongoing","city":"Tucson","state":"AZ","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99631","recalling_firm":"Spectral Instruments Inc","address_1":"420 N Bonita Ave","address_2":"","postal_code":"85745-2747","voluntary_mandated":"FDA Mandated","initial_firm_notification":"","distribution_pattern":"United States.","recall_number":"Z-2939-2026","product_description":"Lago X","product_quantity":"40","reason_for_recall":"Momentary absence of On-Screen \"X-Ray On\" banner during run readiness check.","recall_initiation_date":"20260724","center_classification_date":"20260904","report_date":"20260826","code_info":"All serial numbers.","more_code_info":""},{"status":"Ongoing","city":"Tucson","state":"AZ","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99631","recalling_firm":"Spectral Instruments Inc","address_1":"420 N Bonita Ave","address_2":"","postal_code":"85745-2747","voluntary_mandated":"FDA Mandated","initial_firm_notification":"","distribution_pattern":"United States.","recall_number":"Z-2940-2026","product_description":"Ami HTX","product_quantity":"35","reason_for_recall":"Momentary absence of On-Screen \"X-Ray On\" banner during run readiness check.","recall_initiation_date":"20260724","center_classification_date":"20260904","report_date":"20260826","code_info":"All serial numbers.","more_code_info":""}]}}