{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Priest",
      "state": "N/A",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76494",
      "recalling_firm": "Kiscomedica S.A.",
      "address_1": "Parc Technologique - 2 Place",
      "address_2": "Berthe Morisot",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of MO and country of Switzerland.",
      "recall_number": "Z-1461-2017",
      "product_description": "L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France.    Product Usage:  The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one or two contiguous levels from L2-S1. DDD is defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies. These DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). L-Varlock Lumbar implants are to be used with autogenous bone graft and implanted via an open posterior approach. L-Varlock Lumbar implant is to be used with supplemental fixation. Patients should have at least six (6) months of non-operative treatment prior to treatment with an intervertebral cage.",
      "product_quantity": "13 units",
      "reason_for_recall": "Firm received a complaint of the tip holder breaking during use.",
      "recall_initiation_date": "20170111",
      "center_classification_date": "20170314",
      "report_date": "20170322",
      "code_info": "Batch number: 15486"
    }
  ]
}