{
  "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": "East York",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84844",
      "recalling_firm": "Theralase Inc.",
      "address_1": "41 Hollinger Rd",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "USA; Australia, Bahrain, Canada, Hong Kong Province of China, Jordan, Mexico, Pakistan, Philippines, Thailand, Romania",
      "recall_number": "Z-1353-2020",
      "product_description": "TLC-2000 Therapeutic Medical Laser System",
      "product_quantity": "92 units",
      "reason_for_recall": "660 nm laser diodes may be below rated power output.",
      "recall_initiation_date": "20190926",
      "center_classification_date": "20200224",
      "termination_date": "20201203",
      "report_date": "20200304",
      "code_info": "Serial Numbers: 3245 to 3336 (inclusive)"
    }
  ]
}