{"url_path":"/fda/device/recalls/Z-2354-2026","section_key":"summary","section_title":"DEVICE Recall: Philips North America Llc — DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-01","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Philips North America Llc"},"word_count":81,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2354-2026\n\n**Recalling firm:** Philips North America Llc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-01\n**Report date:** 2026-06-17\n\n## Product\nDigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.\n\n## Reason\nSystem was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.\n\n## Affected lots\nModel Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.\n\n## Distribution\nUS distribution to California."}