{
  "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": "71255",
      "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": "US Nationwide Distribution in the states of CA, TX, FL, NC, MI, GA.",
      "recall_number": "Z-1741-2015",
      "product_description": "Unilateral external fixation ankle clamp    Product Usage:  Unilateral external fixation for use treatment of bone conditions amenable to treatment by use of external fixation modality",
      "product_quantity": "19",
      "reason_for_recall": "Ankle clamp was assembled incorrectly; the offset of the pin to the pivot point is reversed.  This prevents complete range of motion and if pushed too far may loosen the pin from the bone.  A revision surgery may be necessary to adequately reconnect the fixator to the bone.",
      "recall_initiation_date": "20150501",
      "center_classification_date": "20150609",
      "termination_date": "20151208",
      "report_date": "20150617",
      "code_info": "Part 14-450510  Lots:268000, 466170, and 813950"
    }
  ]
}