{
  "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": "West Chester",
      "address_1": "1302 Wrights Ln E",
      "reason_for_recall": "Recall was initiated due to the possibility that the outer pouch was compromised.  The product is packaged in two pouches; a sterile, internal pouch within an external pouch.  It is the outer, external pouch that may be compromised.",
      "address_2": "",
      "product_quantity": "1,011,783",
      "code_info": "Trauma Ex Nails, all lot numbers up to and including lot # 7072305 and Trochanteric Fixation Nails, all lot numbers up to and including lot # 7060897",
      "center_classification_date": "20130826",
      "distribution_pattern": "Nationwide distribution.",
      "state": "PA",
      "product_description": "Synthes Trauma Nail System. The devices are indication for bone fixation.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes USA HQ, Inc.",
      "recall_number": "Z-2058-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65631",
      "termination_date": "20160927",
      "more_code_info": "",
      "recall_initiation_date": "20121102",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}