{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79817",
      "recalling_firm": "Stryker Medical Division of Stryker Corporation",
      "address_1": "3800 E Centre Ave",
      "address_2": "N/A",
      "postal_code": "49002-5826",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Product distributed to the Netherlands",
      "recall_number": "Z-1599-2018",
      "product_description": "6381 M-1 Cot Fastener, catalog no. 6381000000",
      "product_quantity": "3",
      "reason_for_recall": "The Operations Manual and Maintenance Manual are missing various warnings and contain incorrect information.",
      "recall_initiation_date": "20180309",
      "center_classification_date": "20180502",
      "termination_date": "20190409",
      "report_date": "20180509",
      "code_info": "Serial No. 170740538                  170740539                  170740540"
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}