{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Plainsboro",
      "address_1": "666 Plainsboro Rd",
      "reason_for_recall": "CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen impurity, detected in the active ingredient.",
      "address_2": "Bldg 200  Ste 230",
      "product_quantity": "9695 bottles",
      "code_info": "Lot BLM715A, Jul-19",
      "center_classification_date": "20190321",
      "distribution_pattern": "NJ, NY, FL",
      "state": "NJ",
      "product_description": "Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90 count bottles, Rx Only, Manufactured for:  Macleods Pharma USA, Inc., Plainsboro, NJ 08536, Manufactured by:  Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India.  NDC 33342-0052-10",
      "report_date": "20190327",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Macleods Pharma Usa Inc",
      "recall_number": "D-1040-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "82147",
      "termination_date": "20200928",
      "recall_initiation_date": "20190221",
      "postal_code": "08536-3030",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}