{
  "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": [
    {
      "status": "Terminated",
      "city": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65955",
      "recalling_firm": "Synthes USA HQ, Inc.",
      "address_1": "1302 Wrights Ln E",
      "address_2": "",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution, including the states of MI, PA, SC, IA, MA, CA, WI, IL, and KS.",
      "recall_number": "Z-0014-2014",
      "product_description": "Synthes Midfoot Fusion Bolt 6.5 mm.  It is indicated for fracture, fixation, osteotomies, nonunions, and fusions of large bones in the foot and ankle.",
      "product_quantity": "62",
      "reason_for_recall": "A post market safety review following several customer complaints indicated additional clarification was necessary in the Midfoot Fusion Bolt Technique Guide to reduce potential for bolt back-out or migration by emphasizing the need for supplemental fixation.",
      "recall_initiation_date": "20130308",
      "center_classification_date": "20131017",
      "termination_date": "20150812",
      "report_date": "20131023",
      "code_info": "Part Nos.: 04.111.210, 04.111.220, 04.111.230. with Lot Nos.; 2294209 through 7587547.",
      "more_code_info": ""
    }
  ]
}