{
  "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": "206 kits",
      "code_info": "034978C Exp Date 2018-07-09; 038090C Exp Date 2018-09-12; 039153C Exp Date 2018-10-26;",
      "center_classification_date": "20170324",
      "distribution_pattern": "US Distribution to LA and TX.",
      "state": "MO",
      "product_description": "Regard, Item Number: 800567003, Sterile, GY0656C - Robotic Hysterectomy - Alamo",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "recall_number": "Z-1631-2017",
      "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"
    }
  ]
}