{
  "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": "Abbott Park",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "NDA020819"
        ],
        "brand_name": [
          "ZEMPLAR"
        ],
        "generic_name": [
          "PARICALCITOL"
        ],
        "manufacturer_name": [
          "AbbVie Inc."
        ],
        "product_ndc": [
          "0074-1658",
          "0074-4637"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "PARICALCITOL"
        ],
        "rxcui": [
          "200321",
          "213298",
          "352076",
          "1736919",
          "1736921",
          "1736931"
        ],
        "spl_id": [
          "e3e59fde-f50f-49a4-8932-c1f53f579009"
        ],
        "spl_set_id": [
          "7259652f-81bc-4ad1-bba5-d01f9fac1b80"
        ],
        "package_ndc": [
          "0074-4637-01",
          "0074-1658-01",
          "0074-1658-05"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "M0007651",
          "N0000175907",
          "N0000175849"
        ],
        "pharm_class_cs": [
          "Ergocalciferols [CS]"
        ],
        "pharm_class_epc": [
          "Vitamin D2 Analog [EPC]",
          "Vitamin D Analog [EPC]"
        ],
        "unii": [
          "6702D36OG5"
        ]
      },
      "product_type": "Drugs",
      "event_id": "61878",
      "recalling_firm": "Abbott Laboratories",
      "address_1": "100 Abbott Park Rd",
      "address_2": "N/A",
      "postal_code": "60064-3502",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1388-2012",
      "product_description": "Zemplar (paricalcitol) Injection, 5 mcg/mL in 2 mL multi-dose vials, 25 vial carton, Rx only, Manufactured by Hospira, Inc. For Abbott Laboratories, North Chicago, IL 60064, USA, NDC 0074-1658-05",
      "product_quantity": "121,000 vials",
      "reason_for_recall": "CGMP Deviations: There is potential that Abbott's third party manufacturer, Hospira, may have applied a foreign (incorrect) stopper to vials in a specific lot of Zemplar Injection.",
      "recall_initiation_date": "20120514",
      "center_classification_date": "20120618",
      "termination_date": "20121203",
      "report_date": "20120627",
      "code_info": "Lot #: 11-122-DK, Exp 10/13"
    }
  ]
}