{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Elgin",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87231",
      "recalling_firm": "Northgate Technologies, Inc.",
      "address_1": "1591 Scottsdale Ct",
      "address_2": "N/A",
      "postal_code": "60123-9361",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of FL and OH.",
      "recall_number": "Z-1148-2021",
      "product_description": "Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope.",
      "product_quantity": "45 units",
      "reason_for_recall": "An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.",
      "recall_initiation_date": "20210115",
      "center_classification_date": "20210224",
      "termination_date": "20221031",
      "report_date": "20210303",
      "code_info": "Lot Codes:  93830JEK to 93854JEK; 93899LEK to 93908LEK; 93909LEK to 93918LEK"
    }
  ]
}