{
  "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": [
          "ANDA075866"
        ],
        "brand_name": [
          "PORTIA"
        ],
        "generic_name": [
          "LEVONORGESTREL AND ETHINYL ESTRADIOL"
        ],
        "manufacturer_name": [
          "Teva Pharmaceuticals USA, Inc."
        ],
        "product_ndc": [
          "0555-9020"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "rxcui": [
          "238019",
          "748797",
          "748878",
          "751890"
        ],
        "spl_id": [
          "4d63fa4a-ff46-4f2e-b9d5-cab4f5fe1d85"
        ],
        "spl_set_id": [
          "c78b236b-85c4-4258-a524-cea08775100c"
        ],
        "package_ndc": [
          "0555-9020-79",
          "0555-9020-58"
        ],
        "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-245-2013",
      "product_description": "Portia (levonorgestrel and ethinyl estradiol) Tablets, USP, 0.15 mg/0.03 mg, 28-count tablets (containing 21 pink tablets followed by 7 white tablets) per blister card packaged in 6 blister cards per carton, Rx only, Barr Laboratories, Inc., Pomona, NY  10970, NDC 0555-9020-58.",
      "product_quantity": "17,661 blister cards",
      "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 #: 33801951A, and 33802189A, Exp 03/13",
      "more_code_info": ""
    }
  ]
}