{
  "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": "Corona",
      "address_1": "132 Business Center Dr",
      "reason_for_recall": "Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500 mg were found in a sealed 100 count bottle of Oxycodone and Acetaminophen Tablets, USP 10/650 mg lot# 705791A.",
      "address_2": "",
      "product_quantity": "10,615 bottles",
      "code_info": "Lot #: 705791A, Exp 04/2015",
      "center_classification_date": "20131003",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Oxycodone and Acetaminophen Tablets, USP 10 mg/650 mg, CII, 100 Count Bottles, Rx Only, Manufactured by: Watson Laboratories, Inc. Corona, CA 92880 USA, NDC 0591-0825-01",
      "report_date": "20131009",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Watson Laboratories Inc",
      "recall_number": "D-66251-001",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66251",
      "termination_date": "20140725",
      "more_code_info": "",
      "recall_initiation_date": "20130913",
      "postal_code": "92880-1724",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}