{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Charlotte",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83926",
      "recalling_firm": "Monarch Medical Technologies",
      "address_1": "2137 South Blvd Ste 300",
      "address_2": "N/A",
      "postal_code": "28203-5189",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "SC, IL IN, CA",
      "recall_number": "Z-0354-2020",
      "product_description": "EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)",
      "product_quantity": "6 units",
      "reason_for_recall": "Product was distributed prior to approval or clearance from FDA.",
      "recall_initiation_date": "20191001",
      "center_classification_date": "20191108",
      "termination_date": "20260210",
      "report_date": "20191120",
      "code_info": "versions:  v 1.7.1, 1.7.4, 1.7.5"
    }
  ]
}