{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "East York",
      "state": "",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84168",
      "recalling_firm": "Theralase Inc.",
      "address_1": "41 Hollinger Rd",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO,  FL, GA, IL, IN, LA, MD, MN, NC, NJ, NM, NY, OR, WI and countries of AU, BH, CA, HK, JO, MX, PK, PH.",
      "recall_number": "Z-0607-2020",
      "product_description": "TLC-2000 Therapeutic Medical Laser System, Power Pack component TLC-2002  Used for the temporary relief of knee pain.",
      "product_quantity": "306 units",
      "reason_for_recall": "Device was shipped without a Unique Device Identification (UDI) label and a separate label identifies the power pack as CE Marked when the device has not yet received the CE Mark.",
      "recall_initiation_date": "20190926",
      "center_classification_date": "20200218",
      "termination_date": "20201203",
      "report_date": "20191211",
      "code_info": "Serial Numbers on TLC-2002 Power Pack with CE Mark without CE approval:  3012 to 3204, inclusive; and  3202 to 3350 inclusive.    Serial Number 3204 was sold abroad",
      "more_code_info": ""
    }
  ]
}