{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Shirley",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80867",
      "recalling_firm": "Mobius Imaging, LLC",
      "address_1": "2 Shaker Rd Ste F100",
      "address_2": "N/A",
      "postal_code": "01464-2535",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US  and foreign distribution.",
      "recall_number": "Z-2991-2018",
      "product_description": "AIRO Mobile CT System  Model # MobiCT-32",
      "product_quantity": "147",
      "reason_for_recall": "The Tube Current Modulation feature (Modulated Scans) is not working in AIRO systems with software version 2.0.0.0, and operators would not be able to detect this fault until after a scan is completed.",
      "recall_initiation_date": "20180801",
      "center_classification_date": "20180914",
      "termination_date": "20191213",
      "report_date": "20180926",
      "code_info": "Model # MobiCT-32"
    }
  ]
}