{
  "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": "North Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "NDA020263"
        ],
        "brand_name": [
          "LUPRON DEPOT-PED"
        ],
        "generic_name": [
          "LEUPROLIDE ACETATE"
        ],
        "manufacturer_name": [
          "AbbVie Inc."
        ],
        "product_ndc": [
          "0074-2108",
          "0074-2282",
          "0074-2440",
          "0074-3779",
          "0074-9694",
          "0074-3575"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "rxcui": [
          "1115447",
          "1115449",
          "1115454",
          "1115456",
          "1946519",
          "1946520",
          "2639668",
          "2639669",
          "2639742",
          "2639743",
          "2639749",
          "2639750"
        ],
        "spl_id": [
          "24e33d5f-c64b-4d45-a5ae-e18a1f696cfa"
        ],
        "spl_set_id": [
          "e99f47d2-da10-3127-ecb3-e5d942ae6e81"
        ],
        "package_ndc": [
          "0074-2108-03",
          "0074-2282-03",
          "0074-2440-03",
          "0074-3779-03",
          "0074-9694-03",
          "0074-3575-01",
          "0074-3410-01",
          "0074-0010-01"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "300743779035"
        ]
      },
      "product_type": "Drugs",
      "event_id": "67709",
      "recalling_firm": "AbbVie Inc",
      "address_1": "1 N Waukegan Rd",
      "address_2": "",
      "postal_code": "60064",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-1289-2014",
      "product_description": "LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose Administration Kit with prefilled dual-chamber syringe, 11.25 mg for 3-month administration, Rx only, Manufactured for: AbbVie Inc., North Chicago, IL  60064; by: Takeda Pharmaceutical Company Limited, Osaka, Japan 540-8645; NDC 0074-3779-03, UPC 3 00743 77903 5.",
      "product_quantity": "12 kits",
      "reason_for_recall": "Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.",
      "recall_initiation_date": "20140310",
      "center_classification_date": "20140429",
      "termination_date": "20160622",
      "report_date": "20140507",
      "code_info": "Lot #:1013566, Exp 12/08/16",
      "more_code_info": ""
    }
  ]
}