{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-04-22", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "country": "United States", "city": "Andover", "address_1": "3000 Minuteman Rd", "reason_for_recall": "The NBP measurement of Intellivue X3 Patient Monitor shows intermittently only mean values instead of the diastolic and systolic blood pressure values. This is caused by a falsely detected NBP cuff, which is leading to wrong internal NBP setting. 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DE61100853", "center_classification_date": "20180406", "distribution_pattern": "48 Foreign Accounts", "state": "MA", "product_description": "IntelliVue X3 Patient Monitor.", "report_date": "20180418", "classification": "Class II", "openfda": {}, "recalling_firm": "Philips Electronics North America Corporation", "recall_number": "Z-1315-2018", "initial_firm_notification": "Letter", "product_type": "Devices", "event_id": "78732", "termination_date": "20200916", "more_code_info": "", "recall_initiation_date": "20171117", "postal_code": "01810-1032", "voluntary_mandated": "Voluntary: Firm initiated", "status": "Terminated" } ] }