{
  "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": "209 kits",
      "code_info": "027181A Exp Date 2017-03-30; 030175A Exp Date 2017-03-30; 030570A Exp Date 2017-11-30; 031809A Exp Date 2017-12-30; 032419A Exp Date 2018-03-25; 033639A Exp Date 2018-03-30;",
      "center_classification_date": "20170324",
      "distribution_pattern": "US Distribution to LA and TX.",
      "state": "MO",
      "product_description": "Regard, Item Number: 800550001, Sterile, OR0639A - Hip Shoulder - Medical Center Santa Rosa",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Resource Optimization & Innovation Llc",
      "recall_number": "Z-1608-2017",
      "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"
    }
  ]
}