{
  "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": "Ongoing",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91578",
      "recalling_firm": "Stryker Corporation",
      "address_1": "1941 Stryker Way",
      "address_2": "N/A",
      "postal_code": "49002-9711",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1186-2023",
      "product_description": "Triton Canister Software  Catalog Number: GAUS-2.    Intended adjunct in the estimation of blood loss.",
      "product_quantity": "88 units",
      "reason_for_recall": "Triton Canister Software, Insert & Scanning Label  may cause the Triton Canister System to output inaccurate blood loss estimates can lead to confusion and could potentially result in either delayed recognition or prolongation of postpartum hemorrhage (PPH), or require more aggressive treatment for PPH.",
      "recall_initiation_date": "20230125",
      "center_classification_date": "20230227",
      "report_date": "20230308",
      "code_info": "UDI-DI: 00859506006029 Software Version: 2.8.4",
      "more_code_info": ""
    }
  ]
}