{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Selzach",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82140",
      "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": "In the countries of Canada and Korea",
      "recall_number": "Z-0980-2019",
      "product_description": "Instrument Tray, Basic T2 Femur Long  Catalog #: 1806-9900      Product Usage: Knee Arthroplasty",
      "product_quantity": "17 units",
      "reason_for_recall": "The faceplates may incorrectly identify the T2 Basic Long  Instrument Set as T2 Basic Short Instrument Set.",
      "recall_initiation_date": "20190121",
      "center_classification_date": "20190306",
      "termination_date": "20200402",
      "report_date": "20190313",
      "code_info": "Lot Number(s):  K026ACE (lot# packaging)  KU97181 (Vendor code engraved on device)"
    }
  ]
}