{
  "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": "Charlottesville",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73259",
      "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": "E-Mail",
      "distribution_pattern": "Worldwide Distribution.  US nationwide including Puerto Rico, Australia, Bangladesh, Czech Republic, India, Japan, Lebanon, New Zealand, Norway, Singapore, Switzerland, Taiwan, and Turkey.",
      "recall_number": "Z-1323-2016",
      "product_description": "MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration cannula",
      "product_quantity": "37",
      "reason_for_recall": "Complaints that the cannula bent/broke during surgery.",
      "recall_initiation_date": "20160208",
      "center_classification_date": "20160405",
      "termination_date": "20160812",
      "report_date": "20160413",
      "code_info": "0913228216, 0414243005, 0215266350, 0415269875, and 0515271334.",
      "more_code_info": ""
    }
  ]
}