{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Selzach",
      "state": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80131",
      "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": "The products were distributed to the following US states:  AL, Co, FL, KY, NC, TN, UT, and WA.",
      "recall_number": "Z-2393-2018",
      "product_description": "Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S",
      "product_quantity": "12",
      "reason_for_recall": "The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.",
      "recall_initiation_date": "20180427",
      "center_classification_date": "20180710",
      "termination_date": "20200521",
      "report_date": "20180718",
      "code_info": "GTIN 04546540197771; Lot code: K074846",
      "more_code_info": ""
    }
  ]
}