{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Hayward",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "73551",
      "recalling_firm": "Impax Laboratories, Inc.",
      "address_1": "31153 San Antonio Street",
      "address_2": "N/A",
      "postal_code": "94544",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0821-2016",
      "product_description": "Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02",
      "product_quantity": "42,239 HDPE bottles ( 21,119,500 capsules)",
      "reason_for_recall": "Labeling: Incorrect or Missing Lot and/or Exp. Date",
      "recall_initiation_date": "20160317",
      "center_classification_date": "20160414",
      "termination_date": "20161027",
      "report_date": "20160420",
      "code_info": "Lot # 10008320; Exp. 05/16     Lot # 10008744, 10008974; Exp. 11/16   Lot # 10009342; Exp. 03/17    Lot # 10010202; Exp. 09/17     Lot # 20001416A; Exp. 10/17  Lot # 20001557A; Exp. 01/18   Lot # 20001675A; Exp. 03/18   Lot # 20001831A; Exp. 06/18",
      "more_code_info": ""
    }
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}