{
  "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": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83423",
      "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": "US Nationwide Distribution",
      "recall_number": "Z-2416-2019",
      "product_description": "Endotrac EPF/EGR Push Blade, Catalog Number 3053-1     The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.",
      "product_quantity": "251",
      "reason_for_recall": "The seal integrity of the sterile bag containing the kits may be compromised.",
      "recall_initiation_date": "20190725",
      "center_classification_date": "20190827",
      "termination_date": "20200924",
      "report_date": "20190904",
      "code_info": "Lot Numbers 01399, 01464, 01477"
    }
  ]
}