{ "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. 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1) Intera 1.5T Omni/Stellar Model 781104, 2) Intera 1.5T Power/Pulsar Model 781105, 3) Intera 1.5T Master/Nova Model 781106, 4) Intera 1.5T Master CV Model 781107, 5) Intera 1.5T Explorer/ Nova Dual Model 781108, 6) Intera 1.5T IT Model 781160, 7) Intera 1.5T Pulsar Model 781170, 8) Intera 1.5T Achieva Pulsar Model 781171, 9) Intera 1.5T Achieva Nova Model 781172, 10) Intera 1.5T Achieva CV Nova Model 781174, 11) Intera 1.5T Achieva IT Nova Model 781174, 12) Intera 1.5T Achieva I/T Nova Dual Model 781176, 13) Intera 1.5T Model 781195, 14) Intera 1.5T Pulsar New Model 781295, (Added 6/25/18) 15) Intera 1.5T Enterprise", "report_date": "20180425", "classification": "Class II", "openfda": {}, "recalling_firm": "Philips Electronics North America Corporation", "recall_number": "Z-1433-2018", "initial_firm_notification": "Letter", "product_type": "Devices", "event_id": "79451", "termination_date": "20200410", "more_code_info": "", "recall_initiation_date": "20180316", "postal_code": "01810-1032", "voluntary_mandated": "Voluntary: Firm initiated", "status": "Terminated" } ] }