{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tempe",
      "address_1": "720 S Smith Rd",
      "reason_for_recall": "These products are being recalled because they were distributed without adequate labeling and instructions for use.  Inadequate labeling could lead to misuse of the Test Kits and incorrect test results.",
      "address_2": "STE 101",
      "product_quantity": "various quantities",
      "code_info": "Manufacturer's Product Number  HMO-W264    Lot Number  F2290966    Expiration Date:  02/2014",
      "center_classification_date": "20130823",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the country Virgin Islands",
      "state": "AZ",
      "product_description": "SARKEN STAT! Multi-Drug Test Panel    Product Usage- Labeled as \u001cFOR FORENSIC USE ONLY (Employee, Student or Probation Testing)\u001d.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sarken, Inc.",
      "recall_number": "Z-2048-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65841",
      "termination_date": "20140716",
      "more_code_info": "",
      "recall_initiation_date": "20130729",
      "postal_code": "85281-2925",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}