{
  "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": "Leesburg",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87075",
      "recalling_firm": "K2M, Inc",
      "address_1": "600 Hope Pkwy SE",
      "address_2": "",
      "postal_code": "20175-4428",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic: Nationwide     Foreign: Australia, Canada, Netherlands, Singapore",
      "recall_number": "Z-0931-2021",
      "product_description": "Yukon Polyaxial Screw Size  4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System",
      "product_quantity": "248 units/1 each",
      "reason_for_recall": "The Yukon polyaxial screw used in the Yukon Spinal System was incorrectly laser marked with size 5.0 mm (diameter) & 24 mm (length).",
      "recall_initiation_date": "20201214",
      "center_classification_date": "20210127",
      "termination_date": "20230711",
      "report_date": "20210203",
      "code_info": "Product Name / Catalog Number: 7601-04026  Serial/Lot Number(s) Affected: Lot KRBX   Product Code (UDI): 10888857349582",
      "more_code_info": ""
    }
  ]
}