{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Digital templates were created with the incorrect files.",
      "address_2": "",
      "product_quantity": "3232",
      "code_info": "Orthosize Templating Version 1.2.6",
      "center_classification_date": "20170320",
      "distribution_pattern": "Worldwide distribution.  US Nationwide including Puerto Rico, Canada, Argentina, Australia, Austria, Belgium, Chile, China, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Korea, Lithuania, Malaysia, Mexico,  Netherlands, Nicaragua, Norway, Pakistan, Poland, Portugal, Romania, Singapore, South Africa, Spain, Sweden, Switzerland, Turkey, United Kingdom.",
      "state": "IN",
      "product_description": "Orthosize Templating Version 1.2.6  Echo Bi-Metric Hip Stem Digital Templates. For preoperative planning of orthopedic surgery.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1495-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "76442",
      "termination_date": "20171103",
      "more_code_info": "",
      "recall_initiation_date": "20170214",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}