{"url_path":"/fda/device/recalls/Z-2939-2026","section_key":"summary","section_title":"DEVICE Recall: Spectral Instruments Inc — Lago X","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-24","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2939-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Spectral Instruments Inc"},"word_count":50,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2939-2026\n\n**Recalling firm:** Spectral Instruments Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** FDA Mandated\n**Initiated:** 2026-07-24\n**Report date:** 2026-08-26\n\n## Product\nLago X\n\n## Reason\nMomentary absence of On-Screen \"X-Ray On\" banner during run readiness check.\n\n## Affected lots\nAll serial numbers.\n\n## Distribution\nUnited States."}