{"url_path":"/fda/device/recalls/Z-3004-2026","section_key":"summary","section_title":"DEVICE Recall: Merge Healthcare, Inc. — Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation","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-3004-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Merge Healthcare, Inc."},"word_count":69,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3004-2026\n\n**Recalling firm:** Merge Healthcare, Inc.\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\nMerge PACS and Merge OrthoPACS, medical imaging diagnostic workstation\n\n## Reason\nSoftware issue may cause measurements to be displayed inaccurately.\n\n## Affected lots\nSoftware version V9.5 - UDI (01)00842000101239(10)9.5.0(11)260409\n\n## Distribution\nUS Nationwide distribution in the states of California, Florida, Kentucky, Nebraska, Washington."}