{
  "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": [
    {
      "country": "United States",
      "city": "Sellersville",
      "address_1": "650 Cathill Rd",
      "reason_for_recall": "Impurities/Degradation:  This recall is being carried out due to the potential for some lots not meeting impurity specifications.",
      "address_2": "",
      "product_quantity": "100,761 cartons",
      "code_info": "Lot #'s 33800226A, Exp 7/2012; 33800333A, Exp 10/2012; 33800870A, Exp 10/2012; 33802533A, Exp 4/2013; and 33802720A, Exp 8/2013",
      "center_classification_date": "20120626",
      "distribution_pattern": "Nationwide",
      "state": "PA",
      "product_description": "Zeosa (norethindrone and ethinyl estradiol tablets USP, (chewable), 0.4 mg/0.035 mg, and ferrous fumarate tablets USP, (chewable) 75 mg), 3 Blister Cards, 28 Tablets Each, Rx only, TEVA Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-2090-28 and 0093-2090-58, cartons containing three (3) individual blister packs",
      "report_date": "20120704",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Teva Pharmaceuticals USA, Inc.",
      "recall_number": "D-1397-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "61776",
      "termination_date": "20130410",
      "more_code_info": "",
      "recall_initiation_date": "20120502",
      "postal_code": "18960-1512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}