{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Camarillo",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82832",
      "recalling_firm": "Golden State Medical Supply Inc.",
      "address_1": "5187 Camino Ruiz",
      "address_2": "N/A",
      "postal_code": "93012-8601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "IL, MI, MN, PA, TN, TX. Two (2) US government  and one (1) Veterans Affairs accounts. No foreign accounts.",
      "recall_number": "D-1283-2019",
      "product_description": "Losartan Potassium Tablets USP 25 mg 90 count bottle NDC 60429-316-90 Rx only GSMS Incorporated",
      "product_quantity": "64,362 HDPE bottles",
      "reason_for_recall": "CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer",
      "recall_initiation_date": "20190501",
      "center_classification_date": "20190519",
      "termination_date": "20200225",
      "report_date": "20190529",
      "code_info": "GS015172 exp 06/2019   GS017634 02/2020, GS017653 exp 02/2020, GS017980 exp 02/2020,  GS017276 exp 02/2020, GS017045 exp 02/2020,GS016726 exp 02/2020,"
    }
  ]
}