{
  "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": [
    {
      "country": "United States",
      "city": "Libertyville",
      "address_1": "2401 Commerce Dr",
      "reason_for_recall": "CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.",
      "address_2": "",
      "product_quantity": "524 bottles",
      "code_info": "Expiry, lot: 4/30/2019: 8033130; 7/31/2019: 8068192, 8110183, 8080157, 8190195",
      "center_classification_date": "20180818",
      "distribution_pattern": "Nationwide USA",
      "state": "IL",
      "product_description": "Valsartan and Hydrochlorothiazide Tablets, Valsartan 160 MG and Hydrochlorothiazide 12.5 MG, 90 tablets per bottle, Rx Only, MFG: Arrow Pharm (Malta) LTD, Birzebbugia, BBG 3000 Malta. NDC: 54569-6480-0",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "A-S Medication Solutions LLC.",
      "recall_number": "D-1110-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "80748",
      "more_code_info": "",
      "recall_initiation_date": "20180717",
      "postal_code": "60048-4464",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}