{
  "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": "903011225  903011230  903011235  903013225  903013230  903013235",
      "center_classification_date": "20180327",
      "distribution_pattern": "USA (nationwide)",
      "state": "IN",
      "product_description": "ACE Trochanteric Nail System  ACE TROCH NAIL 125 DEG. X 11MM  ACE TROCH NAIL 130 DEG. X 11MM  ACE TROCH NAIL 135 DEG. X 11MM  ACE TROCH NAIL 125 DEG. X 13MM  ACE TROCH NAIL 130 DEG. X 13MM  ACE TROCH NAIL 135 DEG. X 13MM    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-1225-2018",
      "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"
    }
  ]
}