{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Springfield",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72008",
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "address_1": "2909 N Neergard Ave",
      "address_2": "N/A",
      "postal_code": "65803",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to one customer in Lake Charles, LA and one customer in Spartanburg, SC.",
      "recall_number": "Z-2798-2015",
      "product_description": "Regard Custom Surgical Pack, Item Number: 800628; Sterile, CV0805 - CABG B. Used in cardiovascular surgical procedures.",
      "product_quantity": "24 kits",
      "reason_for_recall": "Surgical kits contain a surgical scrub product which may be chemically contaminated and lack sterility assurance.",
      "recall_initiation_date": "20150819",
      "center_classification_date": "20150921",
      "termination_date": "20170405",
      "report_date": "20150930",
      "code_info": "023735"
    }
  ]
}