{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fenton",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91109",
      "recalling_firm": "CoreLink LLC",
      "address_1": "2072 Fenton Logistics Park",
      "address_2": "",
      "postal_code": "63026-2504",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0954-2023",
      "product_description": "CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF:  AT3208",
      "product_quantity": "18 units",
      "reason_for_recall": "Specific lots of FLXfit implants have internal components that may have been manufactured using stainless steel rather than the specified titanium alloy.",
      "recall_initiation_date": "20221020",
      "center_classification_date": "20230112",
      "termination_date": "20240820",
      "report_date": "20230118",
      "code_info": "UDI/DI M725AT32080, Lot Codes:  SM135217, SM129260",
      "more_code_info": ""
    }
  ]
}