{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "It was reported that the number scale/graduation markings were missing on 14 pieces of the swivel clamp.",
      "address_2": "",
      "product_quantity": "49",
      "code_info": "Catalog Number 06350 and Lot Number Identification 994790 (packaged as 042210)",
      "center_classification_date": "20121217",
      "distribution_pattern": "Worldwide Distribution, including the states of TX, TN, PA, CA, NY, FL, and MI and the countries of Japan and Columbia.",
      "state": "IN",
      "product_description": "EBI XFIX DFS Rail System (Adult Rail Gradual Swivel Clamp). The Biomet Rail System consists of a unilateral external fixator rail, modular bone screw clamps, and compression and distraction units. The device is used in the treatment of bone fractures.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-0527-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63725",
      "termination_date": "20130828",
      "more_code_info": "",
      "recall_initiation_date": "20121109",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}