{"url_path":"/fda/device/recalls/Z-3030-2026","section_key":"summary","section_title":"DEVICE Recall: FUJIFILM Healthcare Americas Corporation — FUJIFILM Synapse PACS software v7.4.310; radiological  image processing system","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-22","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3030-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"FUJIFILM Healthcare Americas Corporation"},"word_count":82,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3030-2026\n\n**Recalling firm:** FUJIFILM Healthcare Americas Corporation\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-22\n**Report date:** 2026-09-02\n\n## Product\nFUJIFILM Synapse PACS software v7.4.310; radiological  image processing system\n\n## Reason\nSoftware issue may cause the ruler measurement to be inaccurate.\n\n## Affected lots\nUDI (01)00854904006008(10)0704310, Serial Numbers:  CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38\n\n## Distribution\nWorldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia."}