{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Vicksburg",
      "state": "MS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "79748",
      "recalling_firm": "Kroger Specialty Pharmacy, Inc.",
      "address_1": "100 Pear Orchard Dr Ste A",
      "address_2": "N/A",
      "postal_code": "39180-7153",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MS, LA, AR, IL, FL",
      "recall_number": "D-0762-2018",
      "product_description": "Stelara 90 mg/MI PFS NDC 57894-0061-03 84 days supply",
      "product_quantity": "Unknown",
      "reason_for_recall": "Lack of Processing Controls.",
      "recall_initiation_date": "20180403",
      "center_classification_date": "20180510",
      "termination_date": "20200507",
      "report_date": "20180516",
      "code_info": "All lots remaining within expiry dispensed 12/01/2017 through 02/12/2018"
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}