{
  "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 III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66169",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1061-2013",
      "product_description": "Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.",
      "product_quantity": "875 bottles",
      "reason_for_recall": "Defective Container:  Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.",
      "recall_initiation_date": "20130830",
      "center_classification_date": "20130917",
      "termination_date": "20140725",
      "report_date": "20130925",
      "code_info": "Lot 706224A and 706225A, Exp. 04/15.",
      "more_code_info": ""
    }
  ]
}