{
  "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-1823-2016",
      "product_description": "Various trauma and sports medicine instruments and implants.  Screw, fixation, bone.",
      "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  HAA60-11030  HAA60-13030  HAA60-15040  HAA60-16040  HAA60-18040    Lot #'s  016150  016210  165130  016230  133890  181600  133970  134000  181620"
    }
  ]
}