{
  "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": "Thousand Oaks",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "BLA103234"
        ],
        "brand_name": [
          "PROCRIT"
        ],
        "generic_name": [
          "ERYTHROPOIETIN"
        ],
        "manufacturer_name": [
          "Janssen Products, LP"
        ],
        "product_ndc": [
          "59676-302",
          "59676-303",
          "59676-304",
          "59676-310",
          "59676-340",
          "59676-312",
          "59676-320"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS",
          "SUBCUTANEOUS"
        ],
        "substance_name": [
          "EPOETIN"
        ],
        "rxcui": [
          "205913",
          "205918",
          "205922",
          "205924",
          "212219",
          "213475",
          "239998",
          "239999",
          "240000",
          "240377",
          "241999",
          "242706",
          "1721684",
          "1721690"
        ],
        "spl_id": [
          "325d5d88-413d-28a2-e063-6394a90a3948"
        ],
        "spl_set_id": [
          "0c721ba4-ae19-417f-aae1-221ed1a0866a"
        ],
        "package_ndc": [
          "59676-303-00",
          "59676-303-01",
          "59676-304-00",
          "59676-304-01",
          "59676-310-00",
          "59676-310-01",
          "59676-310-02",
          "59676-302-00",
          "59676-302-01",
          "59676-340-00",
          "59676-340-01",
          "59676-312-00",
          "59676-312-04",
          "59676-320-00",
          "59676-320-04"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "64FS3BFH5W"
        ]
      },
      "product_type": "Drugs",
      "event_id": "77889",
      "recalling_firm": "Amgen, Inc.",
      "address_1": "1 Amgen Center Dr",
      "address_2": "N/A",
      "postal_code": "91320-1730",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States including Puerto Rico",
      "recall_number": "D-1086-2017",
      "product_description": "Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320-1799, Manufactured for: Janssen Products, LP Horsham, PA 19044, NDC 59676-340-01",
      "product_quantity": "175,632 vials",
      "reason_for_recall": "Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.",
      "recall_initiation_date": "20170804",
      "center_classification_date": "20170814",
      "termination_date": "20180329",
      "report_date": "20170823",
      "code_info": "Lot #: G290491A, G290491B, Exp. 06/18"
    }
  ]
}