{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Houston",
      "address_1": "9265 Kirby Dr",
      "reason_for_recall": "Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "all lots within expiry",
      "center_classification_date": "20170523",
      "distribution_pattern": "U.S. Nationwide",
      "state": "TX",
      "product_description": "Calcium Gluconate all strengths, all dosage forms and all packaging, Rx  Only, Avella of Houston, Houston, TX 77054",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Advanced Pharma Inc.",
      "recall_number": "D-0829-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "76561",
      "termination_date": "20171018",
      "more_code_info": "",
      "recall_initiation_date": "20170222",
      "postal_code": "77054-2520",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}