{
  "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": [
    {
      "status": "Terminated",
      "city": "Stamford",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70854",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "419 West Ave",
      "address_2": "N/A",
      "postal_code": "06902-6343",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Distributed in HI.",
      "recall_number": "Z-1585-2015",
      "product_description": "Aspire HD, Full Field Digital, System, x-Ray, Mammographic;  Model: FOR MS-1000.    A mammography system used for screening and diagnosis of breast cancer.",
      "product_quantity": "1 unit",
      "reason_for_recall": "User Manual lacks a description for handling  some errors even though the system can be recovered from such errors",
      "recall_initiation_date": "20150203",
      "center_classification_date": "20150506",
      "termination_date": "20150520",
      "report_date": "20150513",
      "code_info": "Serial Number: 26320119"
    }
  ]
}