{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Stamford",
      "state": "CT",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73709",
      "recalling_firm": "Purdue Pharma L.P.",
      "address_1": "201 Tresser Blvd",
      "address_2": "N/A",
      "postal_code": "06901-3435",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Including: FL, LA, MI, MS, NC, NJ, OH and SC.",
      "recall_number": "D-0810-2016",
      "product_description": "Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg, CIV, 30 Ct Cartons, Rx Only.  Dist by Purdue Pharma L.P., Stamford, CT 06901-3431. NDC: 59011-256-30.",
      "product_quantity": "2172 Cartons",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20160331",
      "center_classification_date": "20160404",
      "termination_date": "20170412",
      "report_date": "20160413",
      "code_info": "Lot #: 3126431B, Expiry: 09/30/17",
      "more_code_info": ""
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}