{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mentor",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90763",
      "recalling_firm": "Steris Corporation Hopkins Facility",
      "address_1": "6515 Hopkins Rd",
      "address_2": "",
      "postal_code": "44060-4307",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in the US only - AK, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MN, MO, MS, NE, NH, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, and WY",
      "recall_number": "Z-1736-2022",
      "product_description": "Verify SixCess Challenge Pack.  Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.",
      "product_quantity": "619 boxes",
      "reason_for_recall": "Product contains incorrect chemical indicators in packaging.",
      "recall_initiation_date": "20220810",
      "center_classification_date": "20220909",
      "termination_date": "20241030",
      "report_date": "20220921",
      "code_info": "UDI-DI (GTIN): 10724995088955  Item Number: LCC003, Lot 3411228A",
      "more_code_info": ""
    }
  ]
}