{
  "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": "Ongoing",
      "city": "Leesburg",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90462",
      "recalling_firm": "K2M, Inc.",
      "address_1": "600 Hope Pkwy Se",
      "address_2": "",
      "postal_code": "20175-4428",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to FL  GA  NE NV  NY  OH OK  SC  Foreign distribution to Canada, EU, and Hong Kong.",
      "recall_number": "Z-1307-2022",
      "product_description": "Yukon Straight Rod  4.0 x120mm;  Cat# 7601-540120.  Used to provide immobilization and stabilization of spinal segments.",
      "product_quantity": "53 devices (19 US; 34 OUS)",
      "reason_for_recall": "Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response; adverse local tissue reactions may occur related to cytotoxicity with the nonconforming rod and surrounding tissue.",
      "recall_initiation_date": "20220613",
      "center_classification_date": "20220630",
      "report_date": "20220706",
      "code_info": "UDI-DI: 10888857326804 Lot PCMW",
      "more_code_info": ""
    }
  ]
}