{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gainesville",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98376",
      "recalling_firm": "Exactech, Inc.",
      "address_1": "2320 Nw 66th Ct",
      "address_2": "N/A",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  CA\tCO\tFL\tGA\tHI\tID\tIL\tIN\tKS\tKY\tLA\tMA\tMD\tME\tMN\tNV\tNY\tOH\tOK\tPR\tSC\tTN\tTX\tVA\tWI  OUS: Australia\tFrance\tGermany\tItaly\tJapan\tKorea\tSpain\tSwitzerland\tUnited Kingdom\tUnited Arab Emirates\tSlovenia",
      "recall_number": "Z-1510-2026",
      "product_description": "Brand Name: Equinoxe   Product Name: Equinoxe Core Instrument Kit  Model/Catalog Number: KIT-311X",
      "product_quantity": "596 kits",
      "reason_for_recall": "Impactor handle may  be missing cross-pin",
      "recall_initiation_date": "20260203",
      "center_classification_date": "20260309",
      "report_date": "20260318",
      "code_info": "All Lots/ UDI-DI: 10885862559166"
    }
  ]
}