{
  "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-0606-2020",
      "product_description": "TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.",
      "product_quantity": "41 units",
      "reason_for_recall": "Device was shipped without a Unique Device Identification (UDI) label.",
      "recall_initiation_date": "20190926",
      "center_classification_date": "20200218",
      "termination_date": "20201203",
      "report_date": "20191211",
      "code_info": "Serial Numbers:  3015, 3022, 3037, 3040, 3047, 3052, 3055, 3074, 3076, 3080, 3100, 3101, 3102, 3103, 3123, 3127, 3129, 3131, 3132, 3137, 3139, 3155, 3162, 3166, 3171, 3183, 3187, 3200, 3206, 3227, 3245, 3266, 3268, 3293, 3296, 3297, 3305, 3308, 3318, 3321, 3332",
      "more_code_info": ""
    }
  ]
}