{
  "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": "903311060  903311065  903311070  903311075  903311080  903311085  903311090  903311095  903311100  903311105  903311110  903311115  903311120  903311125  903311130",
      "center_classification_date": "20180327",
      "distribution_pattern": "USA (nationwide)",
      "state": "IN",
      "product_description": "ACE Trochanteric Nail System  ATN LAG SCREW 60MM STERILE  ATN LAG SCREW 65MM STERILE  ATN LAG SCREW 70MM STERILE  ATN LAG SCREW 75MM STERILE  ATN LAG SCREW 80MM STERILE  ATN LAG SCREW 85MM STERILE  ATN LAG SCREW 90MM STERILE  ATN LAG SCREW 95MM STERILE  ATN LAG SCREW 100MM STERILE  ATN LAG SCREW 105MM STERILE  ATN LAG SCREW 110MM STERILE  ATN LAG SCREW 115MM STERILE  ATN LAG SCREW 120MM STERILE  ATN LAG SCREW 125MM STERILE  ATN LAG SCREW 130MM STERILE        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-1234-2018",
      "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"
    }
  ]
}