{
  "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": "2026-04-29",
    "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": "72053",
      "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": "Product was distributed to one customer in Oklahoma.",
      "recall_number": "Z-0229-2016",
      "product_description": "Regard Custom Surgical Pack, Item Number 880239, Sterile IV Pack.  Custom procedure trays contain surgical instruments and accessories intended for use during a surgical procedure.",
      "product_quantity": "255 packs",
      "reason_for_recall": "The kits contain pressure monitoring kits or sets which are being recalled as a result of flow restriction issues in the trifurcated IV set.",
      "recall_initiation_date": "20150825",
      "center_classification_date": "20151105",
      "termination_date": "20170406",
      "report_date": "20151111",
      "code_info": "Lot 25787E, exp. date 1/19/2017"
    }
  ]
}