{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74038",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and globally to Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecaudor, The Netherlands, Japan, Korea, Malaysia, Mexico, Peru.",
      "recall_number": "Z-1820-2016",
      "product_description": "Various trauma and sports medicine instruments and implants.  Reamer.",
      "product_quantity": "N/A",
      "reason_for_recall": "Insufficient seal strength on sterile barrier packaging.  The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile.  If the product becomes non-sterile and is used or implanted, it may lead to an infection.",
      "recall_initiation_date": "20160401",
      "center_classification_date": "20160526",
      "termination_date": "20170523",
      "report_date": "20160601",
      "code_info": "Part #'s  41009  110004188  110010579    Lot #'s  668490  756990  757010  757030  758180"
    }
  ]
}