{
  "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": [
    {
      "country": "United States",
      "city": "Columbus",
      "address_1": "2550 John Glenn Ave",
      "reason_for_recall": "Failed dissolution specifications",
      "address_2": "Suite A",
      "product_quantity": "925 cartons (30 tablets in each carton)",
      "code_info": "Lot #140849",
      "center_classification_date": "20150616",
      "distribution_pattern": "Nationwide",
      "state": "OH",
      "product_description": "Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "American Health Packaging",
      "recall_number": "D-1140-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "71219",
      "termination_date": "20151009",
      "more_code_info": "",
      "recall_initiation_date": "20150302",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}