{
  "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": "Charlottesville",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76560",
      "recalling_firm": "MicroAire Surgical Instruments, LLC",
      "address_1": "3590 Grand Forks Blvd",
      "address_2": "N/A",
      "postal_code": "22911-9006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States.",
      "recall_number": "Z-1407-2017",
      "product_description": "MicroAire K-Wires",
      "product_quantity": "Total 362",
      "reason_for_recall": "Mislabeling on three lots of K-Wires. The incorrect product description \" dual trocar\" instead of \"single trocar\" was on the product label on the following parts:  1600-9355NS (lot 61005), 1600-9625NS (lot 60297), and 1604-162NS (lot 62856).",
      "recall_initiation_date": "20170221",
      "center_classification_date": "20170303",
      "termination_date": "20170714",
      "report_date": "20170315",
      "code_info": "Part Number, Lot Number, Quantity Distributed to Field  1600-9355NS, 61005,   56; 1600-9625NS, 60297,  209;  1604-162NS, 62856,  97."
    }
  ]
}