{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Selzach",
      "state": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85681",
      "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": "Worldwide distribution - US Nationwide and the countries of   Australia, Austria, Belgium, Canada, Chile, China, France, Germany, Italy, Japan, Netherlands, Poland, South Africa, Spain, Sweden, Switzerland, United Kingdom.  Updated 7/21/20:  Portugal, Denmark, Finland, Norway, Ireland, and Luxembourg.",
      "recall_number": "Z-2376-2020",
      "product_description": "Stryker End Cap, Standard T2 Humerus ¿6 mm\t\t  Catalog Number: 18300003S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.",
      "product_quantity": "109 OUS",
      "reason_for_recall": "Seal integrity of the blister pack may  be compromised and sterility cannot be assured",
      "recall_initiation_date": "20200507",
      "center_classification_date": "20200616",
      "termination_date": "20230921",
      "report_date": "20200624",
      "code_info": "Lot Number: K020793, K020794",
      "more_code_info": ""
    }
  ]
}