{
  "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": {
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    {
      "status": "Terminated",
      "city": "East York",
      "state": "",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84846",
      "recalling_firm": "Theralase Inc.",
      "address_1": "41 Hollinger Rd",
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      "postal_code": "N/A",
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      "initial_firm_notification": "E-Mail",
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      "recall_number": "Z-1266-2020",
      "product_description": "TLC-2000 Therapeutic Medical Laser System",
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      "reason_for_recall": "Laser Probe (Model Number: TLC-2001) Electromagnetic Interference ( EMI ) in excess of IEC-60601-1-2 (4th edition) standard",
      "recall_initiation_date": "20190926",
      "center_classification_date": "20200218",
      "termination_date": "20201203",
      "report_date": "20200226",
      "code_info": "Serial Numbers: 3333 to 3350 (inclusive)",
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