{"recall":{"id":"fda-device-99391","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Merge Healthcare, Inc. recalls 2 products","firm":"Merge Healthcare, Inc.","date":"2026-06-30","reported":"2026-08-12","status":"Ongoing","classification":"Class II","products":[{"name":"Merge PACS, medical imaging diagnostic workstation","code":"UDI (01)00842000101215(10)9.4.0.P01(11)250916, (01)00842000101154(10)9.4.0.P02(11)260302 with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.","quantity":"53 units","number":"Z-2874-2026","classification":"Class II"},{"name":"Merge OrthoPACS, medical imaging diagnostic workstation","code":"UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions: 9.4, 9.4 P01, and 9.4 P02.","quantity":"5 units","number":"Z-2875-2026","classification":"Class II"}],"reason":"Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"Worldwide distribution - US Nationwide and the countries of Canada, and UK.","nationwide":true,"states":[],"units":"53 units; 5 units","remedy":"","whatToDo":"Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.","contact":"","url":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99391","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"40ee5597807436e1","firstSeen":"2026-11-02T13:57:14.206Z","updatedAt":"2026-11-02T13:57:14.206Z","history":[]},"official":{"fetchedAt":"2026-11-02T13:57:14.206Z","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","officialUrl":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99391","record":[{"status":"Ongoing","city":"Hartland","state":"WI","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99391","recalling_firm":"Merge Healthcare, Inc.","address_1":"900 Walnut Ridge Dr","address_2":"","postal_code":"53029-8347","voluntary_mandated":"Voluntary: Firm initiated","initial_firm_notification":"Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit","distribution_pattern":"Worldwide distribution - US Nationwide and the countries of Canada, and UK.","recall_number":"Z-2874-2026","product_description":"Merge PACS, medical imaging diagnostic workstation","product_quantity":"53 units","reason_for_recall":"Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.","recall_initiation_date":"20260630","center_classification_date":"20260804","report_date":"20260812","code_info":"UDI (01)00842000101215(10)9.4.0.P01(11)250916, (01)00842000101154(10)9.4.0.P02(11)260302 with Affected Versions:  9.4, 9.4 P01, and 9.4 P02.","more_code_info":""},{"status":"Ongoing","city":"Hartland","state":"WI","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99391","recalling_firm":"Merge Healthcare, Inc.","address_1":"900 Walnut Ridge Dr","address_2":"","postal_code":"53029-8347","voluntary_mandated":"Voluntary: Firm initiated","initial_firm_notification":"Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit","distribution_pattern":"Worldwide distribution - US Nationwide and the countries of Canada, and UK.","recall_number":"Z-2875-2026","product_description":"Merge OrthoPACS, medical imaging diagnostic workstation","product_quantity":"5 units","reason_for_recall":"Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.","recall_initiation_date":"20260630","center_classification_date":"20260804","report_date":"20260812","code_info":"UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions:  9.4, 9.4 P01, and 9.4 P02.","more_code_info":""}]}}