{
  "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": {
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  "results": [
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      "city": "Tucson",
      "state": "AZ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62452",
      "recalling_firm": "Sunquest Information Systems, Inc.",
      "address_1": "250 S Williams Blvd",
      "address_2": "N/A",
      "postal_code": "85711-4472",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2229-2012",
      "product_description": "Sunquest Laboratory SMART & Sunquest Laboratory SMART Select    Product Usage:  for clinical use",
      "product_quantity": "47 sites",
      "reason_for_recall": "In GUI inquiry, searching by ID (CID) may return the wrong patient demographic data if the accession number associated to the CID is no longer inactive.",
      "recall_initiation_date": "20110812",
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