{
  "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": "74222",
      "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": "The product was distributed in the United States and Sweden",
      "recall_number": "Z-2294-2016",
      "product_description": "Endotine Transbleph 3.5 (CFD-080-0167)",
      "product_quantity": "29",
      "reason_for_recall": "MicroAire has initiated a limited recall (29 Units)on the Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373, due to minor mislabeling ( the front label is correct, but the side label lists an incorrect part number, i.e. CFD-080-0177).",
      "recall_initiation_date": "20160506",
      "center_classification_date": "20160727",
      "termination_date": "20160812",
      "report_date": "20160803",
      "code_info": "Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373"
    }
  ]
}