{
  "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": "Twinsburg",
      "address_1": "1959 Summit Commerce Park",
      "reason_for_recall": "Hitachi discovered a software error that can occur when simultaneously scanning a patient while processing images previously acquired from a different patient. The software error can occur randomly. The error causes an image in the processed dataset to have the same unique identifier (UID) as in the scanning dataset. The processed image is stored in the place of the original image, which is lost.",
      "address_2": "",
      "product_quantity": "45 system units",
      "code_info": "The following serial numbers are associated with this recall:  Echelon - V061, V062, and V065  Oasis - M009, M017, M067, M071, M084, M106-M108, M110-M141 inclusive, and M952  Echelon Oval - Y001-Y005 inclusive",
      "center_classification_date": "20130619",
      "distribution_pattern": "Worldwide Distribution - US Nationwide including the states of  AZ, CA, CO, DE, FL, IL, IN, KS, KY, MD, NC, ND, NY, OH, OR, PA, TX, VA, WA, and WI. One (1) system unit was also distributed to Mexico.",
      "state": "OH",
      "product_description": "Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box.     The Echelon, Echelon Oval and Oasis MR systems are imaging devices, and are intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The MR systems produce transverse, coronal, sagittal, oblique, and curved cross-sectional images that display the internal structure of the head, body, or extremities.",
      "report_date": "20130626",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hitachi Medical Systems America Inc",
      "recall_number": "Z-1559-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65438",
      "termination_date": "20130920",
      "more_code_info": "",
      "recall_initiation_date": "20130131",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}