{
  "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": "Minnetonka",
      "address_1": "5101 Shady Oak Rd S",
      "reason_for_recall": "The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.",
      "address_2": "",
      "product_quantity": "26 units",
      "code_info": "(a) 110470-000, Serial Numbers:  10002845, 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 10003830, 10003243, 10003241, 10002607, 10002848, 10005651, 10007348, 10007424, 10004250, 10004439, 10004576, 10006438, 100030007, 10006887, 10006886  (b) 110470-600, Serial Numbers:  10003244, 10003064, 10003065",
      "center_classification_date": "20180328",
      "distribution_pattern": "US, Canada, China, Australia, Sweden, Germany",
      "state": "MN",
      "product_description": "IMRIS ORT100 Table, Part Numbers:  (a) 110470-000  (b) 110470-600",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Deerfield Imaging, Inc.",
      "recall_number": "Z-1263-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79488",
      "termination_date": "20190912",
      "more_code_info": "",
      "recall_initiation_date": "20180223",
      "postal_code": "55343-4100",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}