{
  "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": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80613",
      "recalling_firm": "Stryker GmbH",
      "address_1": "Bohnackerweg 1",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to KY",
      "recall_number": "Z-2884-2018",
      "product_description": "Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S  T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S  T2 LONG PROXIMAL HUMERAL NAIL LEFT 240mm1832-2824S  T2 LONG PROXIMAL HUMERAL NAIL LEFT 280mm 1832-2828S  T2 LONG PROXIMAL HUMERAL NAIL RIGHT 260mm 1832-3826S  T2 Ankle Arthrd Nail lft 1818-1115S",
      "product_quantity": "38",
      "reason_for_recall": "Incomplete seal on the Tyvek lid  may compromise the sterility of the device",
      "recall_initiation_date": "20180627",
      "center_classification_date": "20180822",
      "termination_date": "20200413",
      "report_date": "20180829",
      "code_info": "Item Number Lot Number:    1819-1020S K0ACFED;  1819-1220S K0CAEC4;   1832-2824S K0BF6C6;   1832-2828S K0CC742;   1832-3826S K0BF6D2;   1818-1115S K0B906C",
      "more_code_info": ""
    }
  ]
}