{
  "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": "69340",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46581",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the state of SD, OH, CT and the country of: The Netherlands and India.",
      "recall_number": "Z-0075-2015",
      "product_description": "Discovery Elbow Humeral Trial     Product Usage:  Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision joint arthoplasty for use in cemented applications. Elbow joint replacement components include humeral and ulnar components, and in some instances, hinge components.",
      "product_quantity": "6",
      "reason_for_recall": "An investigation identified that the product was incorrectly manufactured as a left humeral trial but is etched as a right humeral trial.",
      "recall_initiation_date": "20140924",
      "center_classification_date": "20141016",
      "termination_date": "20150714",
      "report_date": "20141022",
      "code_info": "Catalog Number: 414837  Lot Number: 555011"
    }
  ]
}