{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Twinsburg",
      "address_1": "1959 Summit Commerce Park",
      "reason_for_recall": "The stainless steel belt which runs the length of the table underneath the tabletop is exposed when the tabletop is extended into the magnet for scanning. The firm has received two complaints where technologists have cut their fingers on this belt.",
      "address_2": "",
      "product_quantity": "264",
      "code_info": "M001 to M028, M030 to M108, M110 to M266, M951,  M952",
      "center_classification_date": "20180718",
      "distribution_pattern": "Worldwide Distribution - US Nationwide distribution.in the states of Mexico.",
      "state": "OH",
      "product_description": "Hitachi Oasis MRI system    Product Usage:  Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse, coronal, sagittal, oblique, and curved crosssectional images that display the internal structure of the head, body, or extremities. The images produced by the MR systems reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. The NMR properties that determine the image appearance are proton density, spin-lattice relaxation time (T1), spin-spin relaxation time (T2), and flow. When interpreted by a trained physician, these images provide information that can be useful in diagnosis determination.",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hitachi Medical Systems America Inc",
      "recall_number": "Z-2479-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80464",
      "termination_date": "20200420",
      "more_code_info": "",
      "recall_initiation_date": "20180618",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}