{
  "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": [
    {
      "status": "Terminated",
      "city": "Miami",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85856",
      "recalling_firm": "Neocis Inc.",
      "address_1": "2800 Biscayne Blvd Ste 600",
      "address_2": "N/A",
      "postal_code": "33137-4523",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including in the states of AZ, CA, FL, NY, and NH",
      "recall_number": "Z-2639-2020",
      "product_description": "DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.",
      "product_quantity": "50 units",
      "reason_for_recall": "The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.",
      "recall_initiation_date": "20200514",
      "center_classification_date": "20200716",
      "termination_date": "20210727",
      "report_date": "20200722",
      "code_info": "Work Order (lot): 1623"
    }
  ]
}