{
  "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": "216 kits",
      "code_info": "026440A Exp Date 2017-07-16; 030021A Exp Date 2017-12-11; 030186A Exp Date 2017-12-21; 031464A Exp Date 2018-02-15; 032390A Exp Date 2018-03-22; 033782A Exp Date 2018-05-20",
      "center_classification_date": "20170324",
      "distribution_pattern": "US Distribution to LA and TX.",
      "state": "MO",
      "product_description": "Regard, Item Number: 800417001, Sterile, GY0486A - Laparoscopy Pk - Spohn",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "recall_number": "Z-1657-2017",
      "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"
    }
  ]
}