{
  "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": "2026-04-22",
    "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": "66967",
      "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": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - USA Nationwide and in the countries of Europe, Italy, UK, Australia, Japan.  all product in USA is under Biomet control.",
      "recall_number": "Z-0493-2014",
      "product_description": "G7 Acetabular Screw 6.5mmx35mm  Part Number: 010001000",
      "product_quantity": "532 in USA all under Biomet USA control",
      "reason_for_recall": "Investigation identified that the outer label, inner label, and patient label all have the incorrect diameter size of 10.5mm. The screw is actually a 6.5mm diameter and correctly corresponds to the items number on the label.",
      "recall_initiation_date": "20131126",
      "center_classification_date": "20131226",
      "termination_date": "20140929",
      "report_date": "20140101",
      "code_info": "Lot Numbers: 3070517, 3070528, 3077748, 3077750, 3077751, 3085183, 3105038, 3123395, 3123398, 3123399,  3123400, 3146439, 3165497, 3165498, 3165499, 3165500, 3181736",
      "more_code_info": ""
    }
  ]
}