{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89588",
      "recalling_firm": "Nextremity Solutions",
      "address_1": "1195 Polk Dr",
      "address_2": "N/A",
      "postal_code": "46582-8602",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.",
      "recall_number": "Z-0740-2022",
      "product_description": "Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe  SKU: CH-STD-KT",
      "product_quantity": "24 units",
      "reason_for_recall": "During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision",
      "recall_initiation_date": "20220113",
      "center_classification_date": "20220309",
      "termination_date": "20240524",
      "report_date": "20220316",
      "code_info": "Lot Numbers: 1574701, 158961  UDI: 00817701026372"
    }
  ]
}