{
  "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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    {
      "status": "Terminated",
      "city": "Pulaski",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76617",
      "recalling_firm": "AVKARE Inc.",
      "address_1": "615 N 1st St",
      "address_2": "",
      "postal_code": "38478-2403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0610-2017",
      "product_description": "Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for:  AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13",
      "product_quantity": "116 cartons",
      "reason_for_recall": "Failed impurities/ degradation specifications: Product was above specification for unknown impurities.",
      "recall_initiation_date": "20170215",
      "center_classification_date": "20170322",
      "termination_date": "20220601",
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      "code_info": "Lot #15152, Exp. 02/2018",
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}