{
  "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": "Failed Tablet/Capsule Specifications; Product contains broken tablets.",
      "address_2": "",
      "product_quantity": "717 bottles",
      "code_info": "Lot #: 697316A, Expiry: Mar 2015.",
      "center_classification_date": "20140130",
      "distribution_pattern": "Nationally in: AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI.",
      "state": "CA",
      "product_description": "Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only.  Manufactured by Watson Laboratories, Inc., Corona, CA 92880.  Distributed by: Watson Pharma, Inc. NDC: 00591-0517-01.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Watson Laboratories Inc",
      "recall_number": "D-1053-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "67348",
      "termination_date": "20140725",
      "more_code_info": "",
      "recall_initiation_date": "20140115",
      "postal_code": "92880-1724",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}