{
  "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": "2026-04-15",
    "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": "71904",
      "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": "Distribution was made to LA, MS, and TX.",
      "recall_number": "Z-0104-2016",
      "product_description": "regard Item Number: 880327002, sterile, CV0758B - Open Heart A&B -  surgical kit containing cover light handle soft, RX.  The responsible firm on the label is ROi, LLC, St. Louis, MO.  Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure",
      "product_quantity": "36 kits",
      "reason_for_recall": "The kits contain an equipment glove component which may contain splits or holes compromising the sterility.",
      "recall_initiation_date": "20150422",
      "center_classification_date": "20151007",
      "termination_date": "20170328",
      "report_date": "20151014",
      "code_info": "Lot numbers 24298 and 24572."
    }
  ]
}