{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92078",
      "recalling_firm": "Wright Medical Technology, Inc.",
      "address_1": "1023 Cherry Rd",
      "address_2": "N/A",
      "postal_code": "38117-5423",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1466-2023",
      "product_description": "stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation",
      "product_quantity": "41 units",
      "reason_for_recall": "Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.",
      "recall_initiation_date": "20230410",
      "center_classification_date": "20230426",
      "report_date": "20230503",
      "code_info": "UDI/DI 00889797101011, Lot Number 1736809"
    }
  ]
}