{
  "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-1120-2015",
      "product_description": "Bimix (PHENT;PAP) (N), solution, (10/300) 1 - 30 mg/mL, injectable, 5ml vial, Rx only, compounded by Montana Compounding Pharmacy in Missoula, MT.",
      "product_quantity": "1/5mL vial",
      "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 04102015:18@15, expiry date: 7/3/2015"
    }
  ]
}