{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cedar Park",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65953",
      "recalling_firm": "Specialty Compounding, LLC",
      "address_1": "211 South Bell (Hwy 183 N)",
      "address_2": "N/A",
      "postal_code": "78613",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0231-2015",
      "product_description": "All products, Rx Only Manufactured by Specialty Compounding, 211 S. Bell Blvd, Cedar Park, TX 78613",
      "product_quantity": "Undetermined",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20130809",
      "center_classification_date": "20141030",
      "termination_date": "20160922",
      "report_date": "20141105",
      "code_info": "ALL lots of product on the market as of August 9, 2013.",
      "more_code_info": ""
    }
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}