{
  "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": "86748",
      "recalling_firm": "K2M, Inc",
      "address_1": "600 Hope Pkwy SE",
      "address_2": "N/A",
      "postal_code": "20175-4428",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0520-2021",
      "product_description": "Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the  Alignment Tube ) provides counter rotation to reduce the torque applied to the anatomy when the size 15 Torque limiting shaft (the  shaft  is used to tighten the Yukon Set Screw to the specified torque.",
      "product_quantity": "4 devices",
      "reason_for_recall": "Shafts do not pass through the inner cannula of the Anti-Torque Alignment Tube from Lot KTGG due to a manufacturing nonconformance. This could result in a delay of surgery or result in surgical intervention later on.",
      "recall_initiation_date": "20201103",
      "center_classification_date": "20201202",
      "termination_date": "20210112",
      "report_date": "20201209",
      "code_info": "Catalog Number/REF 7601-90001  LOT KTGG  GTIN 10888857343948",
      "more_code_info": ""
    }
  ]
}