{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "6210 N Buffalo St",
      "reason_for_recall": "Proximal end of the driver in the affected product  may be oversized in varying degrees, potentially making it difficult to connect with and remove from the proximal Nextra implant",
      "address_2": "",
      "product_quantity": "190 units",
      "code_info": "Lot Number: 168117318B  UDI: 00817701020011",
      "center_classification_date": "20200309",
      "distribution_pattern": "International distribution in the countries of Spain, United Kingdom, Germany, and Switzerland.",
      "state": "IN",
      "product_description": "Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile.  REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes.",
      "report_date": "20200318",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nextremity Solutions",
      "recall_number": "Z-1458-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84924",
      "termination_date": "20201217",
      "more_code_info": "",
      "recall_initiation_date": "20200212",
      "postal_code": "46580",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}