{
  "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": "Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw Blade Assembly was identified as CAM Assembly.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Lot 669420",
      "center_classification_date": "20140320",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to states of: NY, TX, MI, and M; to countries of: Australia and The Netherlands.",
      "state": "IN",
      "product_description": "Part 475620 Intramedullary Bone Saw CAM Assembly   Size 12mm,     A unique and exclusive clinical instrument used to correct leg length, or rotational discrepancies in the femur.",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-1242-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "67618",
      "termination_date": "20150707",
      "more_code_info": "",
      "recall_initiation_date": "20140226",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}