{
  "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": {
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      "country": "United States",
      "city": "Camarillo",
      "address_1": "5187 Camino Ruiz",
      "reason_for_recall": "CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.",
      "address_2": "",
      "product_quantity": "14,955 bottles (1,345,950 tablets)",
      "code_info": "Lot #: GS017651, Expiration 01/2020",
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      "distribution_pattern": "US Nationwide One (1) US government account. No foreign accounts.",
      "state": "CA",
      "product_description": "Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90",
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      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Golden State Medical Supply Inc.",
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      "recall_initiation_date": "20190614",
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