{
  "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": "88630",
      "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": "Letter",
      "distribution_pattern": "Domestic distribution to CO, IL, LA, MA, MS, OK, PA, TN, and TX. Foreign distribution to Columbia, UK, Netherlands, and Canada.",
      "recall_number": "Z-0104-2022",
      "product_description": "Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068",
      "product_quantity": "23",
      "reason_for_recall": "Units may arrive with missing pins and/or in a state in disassembly. Pins dislodging from the instrument during a procedure may enter the surgical cavity, requiring intraoperative removal or revision surgery.",
      "recall_initiation_date": "20210908",
      "center_classification_date": "20211013",
      "termination_date": "20240517",
      "report_date": "20211020",
      "code_info": "Lots CCUNA, HYMJ, KNCU"
    }
  ]
}