{
  "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": "Fort Mill",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86178",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "785 Fort Mill Hwy",
      "address_2": "N/A",
      "postal_code": "29707-7555",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution including the state of North Carolina.",
      "recall_number": "Z-3016-2020",
      "product_description": "KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.",
      "product_quantity": "9,150 kits",
      "reason_for_recall": "Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.",
      "recall_initiation_date": "20200730",
      "center_classification_date": "20200925",
      "termination_date": "20210428",
      "report_date": "20201007",
      "code_info": "Model:  ORPDH5994A  Lot numbers:  558357, 561502,566549, 571467, 574058.    Expiration dates: Varies by kit components."
    }
  ]
}