{
  "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": [
    {
      "country": "United States",
      "city": "Corona",
      "address_1": "595 N Smith Ave",
      "reason_for_recall": "Presence of Foreign Tablets/Capsules",
      "address_2": "",
      "product_quantity": "450 bottles",
      "code_info": "NDC 33261-0715-00    Batch ID:  57909-1, exp. date 04/30/2019  57909-2, exp. date 06/30/2019",
      "center_classification_date": "20180515",
      "distribution_pattern": "Product was distributed to Florida",
      "state": "CA",
      "product_description": "Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00",
      "report_date": "20180523",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Aidarex Pharmaceuticals LLC",
      "recall_number": "D-0810-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "79835",
      "termination_date": "20191204",
      "more_code_info": "",
      "recall_initiation_date": "20180410",
      "postal_code": "92880-6920",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}