{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Louis",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "NDA020124"
        ],
        "brand_name": [
          "DIAZEPAM"
        ],
        "generic_name": [
          "DIAZEPAM"
        ],
        "manufacturer_name": [
          "Meridian Medical Technologies LLC"
        ],
        "product_ndc": [
          "11704-600"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR"
        ],
        "substance_name": [
          "DIAZEPAM"
        ],
        "rxcui": [
          "1807452"
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        "spl_id": [
          "9e08d47f-b706-44b2-9e2f-9ca972592050"
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        "spl_set_id": [
          "fa352464-14c8-49e9-b8b7-5a968b1cfa93"
        ],
        "package_ndc": [
          "11704-600-01"
        ],
        "is_original_packager": [
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        "upc": [
          "0311704600015"
        ],
        "nui": [
          "N0000175694",
          "M0002356"
        ],
        "pharm_class_epc": [
          "Benzodiazepine [EPC]"
        ],
        "pharm_class_cs": [
          "Benzodiazepines [CS]"
        ],
        "unii": [
          "Q3JTX2Q7TU"
        ]
      },
      "product_type": "Drugs",
      "event_id": "62015",
      "recalling_firm": "Meridian Medical Technologies a Pfizer Company",
      "address_1": "1945 Craig Rd",
      "address_2": "",
      "postal_code": "63146-4105",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide, military, Italy, Singapore, Sweden, and Canada.",
      "recall_number": "D-1369-2012",
      "product_description": "Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15-count autoinjectors per carton, Rx only, Meridian Medical Technologies, Columbia, MD  21046; A subsidiary of King Pharmaceuticals, Inc.; NSN 6505-01-274-0951, NDC 11704-600-01.",
      "product_quantity": "83,400 autoinjectors",
      "reason_for_recall": "Impurities/Degradation Products: High Out of Specification levels for carbostyril, a known degradation product of diazepam.",
      "recall_initiation_date": "20120606",
      "center_classification_date": "20120611",
      "termination_date": "20130805",
      "report_date": "20120620",
      "code_info": "Lot #: 8D1082, Exp 01/13; 8D1151, Exp 03/13",
      "more_code_info": ""
    }
  ]
}