{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89764",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution US Nationwide, Japan, and the Netherlands",
      "recall_number": "Z-0912-2022",
      "product_description": "Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit   SKU: NX-3532K   Orthopedic surgical instrument",
      "product_quantity": "285 units",
      "reason_for_recall": "Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery",
      "recall_initiation_date": "20220210",
      "center_classification_date": "20220412",
      "termination_date": "20241010",
      "report_date": "20220420",
      "code_info": "Lot Number: 168125017A UDI:  00817701020042"
    }
  ]
}