{
  "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": "1,548 kits",
      "code_info": "026446A Exp Date 2017-07-16; 030247A Exp Date 2017-12-28; 032384A Exp Date 2018-03-22; 033038A Exp Date 2018-04-20; 034310A Exp Date 2018-06-17;",
      "center_classification_date": "20170324",
      "distribution_pattern": "US Distribution to LA and TX.",
      "state": "MO",
      "product_description": "Regard, Item Number: 880326001, Sterile, GS0757A  - Major Basin - OSU",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "recall_number": "Z-1562-2017",
      "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"
    }
  ]
}