{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Broomfield",
      "address_1": "310 Interlocken Pkwy Ste 120",
      "reason_for_recall": "The outer diameter of the Drill shaft is oversized; thereby, resulting in interference fit when inserting the Drill into the Fixed or Variable Sleeve Assembly.",
      "address_2": "",
      "product_quantity": "15",
      "code_info": "Model 8630-0102 Anchored Lateral Retractable Drill lot TU00049: February 25, 2013 and TU00155: July 31, 2013",
      "center_classification_date": "20150115",
      "distribution_pattern": "Distributed in PR and the states of NY, AZ, TN, TX, and CA.",
      "state": "CO",
      "product_description": "Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102.     Timberline Anchored Lateral Retractable Drills are used with the Timberline MPF System to establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet Spine, LLC",
      "recall_number": "Z-0982-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70056",
      "termination_date": "20150313",
      "more_code_info": "",
      "recall_initiation_date": "20130822",
      "postal_code": "80021-3464",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}