{
  "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": "72106",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-2821-2015",
      "product_description": "ASP-1020\tLipoTower with Aspiration Pump.  Medical use.",
      "product_quantity": "3 LipoTower with Aspiration Pump",
      "reason_for_recall": "There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.",
      "recall_initiation_date": "20150612",
      "center_classification_date": "20150930",
      "termination_date": "20160523",
      "report_date": "20151007",
      "code_info": "Serial numbers 14031102, 15021105, and 14101103."
    }
  ]
}