{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Pulaski",
      "state": "TN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82564",
      "recalling_firm": "AVKARE Inc.",
      "address_1": "615 N 1st St",
      "address_2": "N/A",
      "postal_code": "38478-2403",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "D-1122-2019",
      "product_description": "Telmisartan and Amlodipine Tablets 80 mg/5 mg, 30 tablets,  Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478 --- NDC 42291-795-30",
      "product_quantity": "397 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications; 18 month long term stability study (manufacturer)",
      "recall_initiation_date": "20190403",
      "center_classification_date": "20190411",
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      "report_date": "20190417",
      "code_info": "Lots: 201916 Exp. 08/2019; 20092 Exp. 08/2019"
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