{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for the ATN system.",
      "address_2": "",
      "product_quantity": "3454",
      "code_info": "903208000  903208010  903208015  903208020  903208025",
      "center_classification_date": "20180327",
      "distribution_pattern": "USA (nationwide)",
      "state": "IN",
      "product_description": "ACE Trochanteric Nail System  STER TROC END CAP  STER TROC END CAP 5MM  STER TROC END CAP 10MM  STER TROC END CAP 15MM  STER TROC END CAP 20MM  STER TROC END CAP 25MM    The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, intertrochanteric fractures, high subtrochanteric fractures and combinations of these fractures. The Trochanteric Long Nail System is additionally indicated to treat pertrochanteric fractures associated with shaft fractures, pathologic fractures in osteoporotic bone of the trochanteric and diaphyseal areas, long subtrochanteric fractures, ipsilateral femoral fractures, proximal or distal nonunions and malunions and revision procedures.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1226-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79408",
      "termination_date": "20200422",
      "more_code_info": "",
      "recall_initiation_date": "20171220",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}