{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Missoula",
      "state": "MT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71275",
      "recalling_firm": "Montana Compounding Pharmacy",
      "address_1": "111 N Higgins Ave",
      "address_2": "N/A",
      "postal_code": "59802-4437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MT and ND",
      "recall_number": "D-1125-2015",
      "product_description": "Trimix (A;PH,PA) (N), injectable, 160 UG-1.2 mg-9.6/ mg/mL, 2 mL vial, Rx only, compounded by Montana Compounding Pharmacy, Missoula, MT.",
      "product_quantity": "32/2 mL vials",
      "reason_for_recall": "Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection",
      "recall_initiation_date": "20150515",
      "center_classification_date": "20150609",
      "termination_date": "20161220",
      "report_date": "20150617",
      "code_info": "Lot 02112015:78@15, expiry dates:  6/1/2015;  Lot 04062015:03@9, expiry dates: 6/8/2015"
    }
  ]
}