{"url_path":"/fda/device/recalls/Z-3036-2026","section_key":"summary","section_title":"DEVICE Recall: GE Medical Systems Information Technologies Inc — PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-20","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3036-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"GE Medical Systems Information Technologies Inc"},"word_count":135,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3036-2026\n\n**Recalling firm:** GE Medical Systems Information Technologies Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-20\n**Report date:** 2026-09-02\n\n## Product\nPORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209\n\n## Reason\nSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.\n\n## Affected lots\nGTIN 00195278679284, Serial Numbers:  SWT25250001TA, SWT25360001TA, SWT25360002TA, SWT24090006TA, SWT25100001TA, SWT25120002TA, SWT24140007TA, SWT24150008TA, SWT25100004TA, SWT24050001TA, SWT25110003TA, SWT24180011TA, SWT25120003TA, SWT25230001TA, SWT25230002TA, SWT25110009TA, SWT25110010TA, SWT25230003TA, SWT25230005TA, SWT25230006TA, SWT25230004TA, SWT25260001TA, SWT31240012TA.\n\n## Distribution\nUS:  MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom."}