{
  "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": "Zanesville",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70334",
      "recalling_firm": "Cardinal Health",
      "address_1": "3540 East Pike",
      "address_2": "N/A",
      "postal_code": "43701-9526",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "OK",
      "recall_number": "D-0489-2015",
      "product_description": "Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by Upsher-Smith Laboratories, Inc. Minneapolis, MN 55447 for Sandoz, Inc., Princeton, NJ 08540 Repackaged by Cardinal Health Zanesville, OH 43701",
      "product_quantity": "100 blister cards",
      "reason_for_recall": "Labeling: Incorrect or Missing Package Insert: the package insert for the potassium chloride 8 mEq and 10 mEq strength instead of the potassium chloride 10 mEq and 20 mEq strength was packaged with the product.",
      "recall_initiation_date": "20131002",
      "center_classification_date": "20150415",
      "termination_date": "20150930",
      "report_date": "20150422",
      "code_info": "Lot #: 315004A,  Exp 1/15/14; Lot #: 315620A,  Exp 1/15/14"
    }
  ]
}