{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Burlington",
      "state": "Ontario",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80392",
      "recalling_firm": "Wescam Inc",
      "address_1": "649 North Service Rd",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide  Distribution",
      "recall_number": "Z-2316-2018",
      "product_description": "MX-10 surveillance laser system    Product Usage:  The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.",
      "product_quantity": "29",
      "reason_for_recall": "Product has a nominal ocular hazard distance (NOHD) that is longer than specified and persons could be exposed to light in excess of the exposure limit.",
      "recall_initiation_date": "20180508",
      "center_classification_date": "20180715",
      "termination_date": "20210824",
      "report_date": "20180725",
      "code_info": "L3 Wescam MX-10, part numbers 44620-203, 44620-211, 44620-213, 44620-215, 44620-221,4620-258, 44620-263, 44620-277, 45840-13, 45840-20, and 45840-23",
      "more_code_info": ""
    }
  ]
}