{
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    "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": "Columbus",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73715",
      "recalling_firm": "Amerisource Health Services",
      "address_1": "2550 John Glenn Ave",
      "address_2": "Suite A",
      "postal_code": "43217-1188",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0823-2016",
      "product_description": "Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 Carton of 30:NDC 68084-835-32, Individual Dose: NDC 68084-835-33.",
      "product_quantity": "5,034 cartons (151,020 capsules)",
      "reason_for_recall": "Labeling: Incorrect or Missing Lot and/or Exp Date",
      "recall_initiation_date": "20160331",
      "center_classification_date": "20160414",
      "termination_date": "20170111",
      "report_date": "20160420",
      "code_info": "Lot #142548; Exp. 05/16  Lot #145036; Exp. 10/16  Lot #151170; Exp. 03/17   Lot #152978; Exp. 09/17   Lot #155080; Exp. 01/18.",
      "more_code_info": ""
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}