{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88399",
      "recalling_firm": "Clarus Medical, Llc",
      "address_1": "13355 10th Ave N Ste 110",
      "address_2": "N/A",
      "postal_code": "55441-5554",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in US - 18 accounts 1 foreign account",
      "recall_number": "Z-2405-2021",
      "product_description": "Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002",
      "product_quantity": "858 units",
      "reason_for_recall": "The sterile barrier seal may be compromised.",
      "recall_initiation_date": "20210727",
      "center_classification_date": "20210902",
      "termination_date": "20220915",
      "report_date": "20210908",
      "code_info": "Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022"
    }
  ]
}