{
  "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": [
    {
      "country": "United States",
      "city": "Miami",
      "address_1": "530 NW 29th St",
      "reason_for_recall": "The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.",
      "address_2": "",
      "product_quantity": "100 units",
      "code_info": "Work Order (Lot) Number 1573",
      "center_classification_date": "20210126",
      "distribution_pattern": "OH, FL, CT, MA, AZ PA, NY",
      "state": "FL",
      "product_description": "DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis Guidance System (NGS)",
      "report_date": "20210203",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Neocis, Inc.",
      "recall_number": "Z-0929-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "87060",
      "termination_date": "20210811",
      "more_code_info": "",
      "recall_initiation_date": "20201030",
      "postal_code": "33127-3917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}