{
  "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": "Corona",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66360",
      "recalling_firm": "Watson Laboratories Inc",
      "address_1": "132 Business Center Dr",
      "address_2": "N/A",
      "postal_code": "92880-1724",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US. No international.  NATIONWIDE",
      "recall_number": "D-66360-001",
      "product_description": "Next Choice\" One Dose Emergency Contraceptive (Levonorgestrel Tablet), 1.5 mg, 1 Tablet/Blister Card (NDC 52544-287-54), Manufactured by Watson Laboratories Inc, 132 Business Center Drive, Corona, CA 92880.",
      "product_quantity": "1,002,394 tablets",
      "reason_for_recall": "Failed Tablet/Capsule Specifications: Multiple complaints for push through tablet breakage.",
      "recall_initiation_date": "20130923",
      "center_classification_date": "20131009",
      "termination_date": "20140725",
      "report_date": "20131016",
      "code_info": "Lot#: 580974AA and 580975AA.  Exp: 09/14"
    }
  ]
}