{
  "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": "Sellersville",
      "state": "PA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "NDA021544"
        ],
        "brand_name": [
          "JOLESSA"
        ],
        "generic_name": [
          "LEVONORGESTREL / ETHINYL ESTRADIOL"
        ],
        "manufacturer_name": [
          "Teva Pharmaceuticals USA, Inc."
        ],
        "product_ndc": [
          "0555-9123"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "rxcui": [
          "238019",
          "748797",
          "751901",
          "762663"
        ],
        "spl_id": [
          "aaf5797d-3069-42ba-a8d2-088e5cd33b2c"
        ],
        "spl_set_id": [
          "f1076019-6f2c-4c90-9f3c-ab0c7cdd9315"
        ],
        "package_ndc": [
          "0555-9123-66"
        ],
        "is_original_packager": [
          true
        ]
      },
      "product_type": "Drugs",
      "event_id": "64607",
      "recalling_firm": "Teva Pharmaceuticals USA, Inc.",
      "address_1": "650 Cathill Rd",
      "address_2": "",
      "postal_code": "18960-1512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-246-2013",
      "product_description": "Jolessa (levonorgestrel/ethinyl estradiol) Tablets, 0.15 mg/0.03 mg, 91-count tablets per extended-cycle tablet dispenser packaged in 3 dispensers per carton, Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY  10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA  18960, NDC 0555-9123-66.",
      "product_quantity": "71,893 dispensers",
      "reason_for_recall": "Failed Tablet/Capsule Specifications: This recall is being carried out due to an out of specification result for appearance.",
      "recall_initiation_date": "20130312",
      "center_classification_date": "20130410",
      "termination_date": "20140115",
      "report_date": "20130417",
      "code_info": "Lot #: 33803603A, 33803604A, Exp 11/13; 33803996A, and 33803997A, Exp 03/14",
      "more_code_info": ""
    }
  ]
}