{
  "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": "Orange City",
      "address_1": "PO Box 320",
      "reason_for_recall": "When using the recalled product in split shift mode, the non-sub-millimeter positioning has been found to be inconsistent with the setting parameters.",
      "address_2": "1401 8th St SE",
      "product_quantity": "9",
      "code_info": "Versions 1.6.1 (Part Number MT6XSM1.6.1), 1.7.0 (Part Number MT6XSM1.7.0), and 1.7.1 (Part Number MT6XSM1.7.1)",
      "center_classification_date": "20160615",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the countries of  Switzerland, Germany..",
      "state": "IA",
      "product_description": "Protura Robotic Couch System Software, versions 1.6.1 (Part Number MT6XSM1.6.1), 1.7.0 (Part Number MT6XSM1.7.0), and 1.7.1 (Part Number MT6XSM1.7.1), CIVCO, Orange City, IA 51041",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Med Tec Inc",
      "recall_number": "Z-1992-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73692",
      "termination_date": "20170203",
      "more_code_info": "",
      "recall_initiation_date": "20160331",
      "postal_code": "51041-7463",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}