{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Selzach",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82894",
      "recalling_firm": "Stryker GmbH",
      "address_1": "Bohnackerweg 1",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed US nationwide.",
      "recall_number": "Z-1849-2019",
      "product_description": "Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1",
      "product_quantity": "1600",
      "reason_for_recall": "The seal integrity of the sterile bag containing the kits may be compromised.",
      "recall_initiation_date": "20190430",
      "center_classification_date": "20190620",
      "termination_date": "20200918",
      "report_date": "20190626",
      "code_info": "Lot #s 01404, 01478"
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}