{
  "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": [
    {
      "country": "United States",
      "city": "Springfield",
      "address_1": "2909 N Neergard Ave",
      "reason_for_recall": "Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.",
      "address_2": "",
      "product_quantity": "249 kits",
      "code_info": "035084B Exp Date 2018-07-13; 038325B Exp Date 2018-09-22; 039576B Exp Date 2018-11-12",
      "center_classification_date": "20170324",
      "distribution_pattern": "US Distribution to LA and TX.",
      "state": "MO",
      "product_description": "Regard, Item Number: 800416002, Sterile, GY0485B - Robotic Hysterectomy Pk - Spohn",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "recall_number": "Z-1656-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "76255",
      "termination_date": "20180928",
      "more_code_info": "",
      "recall_initiation_date": "20170109",
      "postal_code": "65803-6317",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}