{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "cfres_id": "173298",
      "product_res_number": "Z-1783-2019",
      "event_date_initiated": "2019-01-29",
      "event_date_created": "2019-06-28",
      "recall_status": "Open, Classified",
      "res_event_number": "82988",
      "product_code": "RET",
      "product_description": "TASE 400 Imaging systems",
      "code_info": "TASE 400",
      "firm_fei_number": "3021214229",
      "recalling_firm": "COLLINS AEROSPACE",
      "address_1": "9 Technology Park Dr",
      "city": "Westford",
      "state": "MA",
      "postal_code": "01886-3141",
      "reason_for_recall": "the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Collins Aerospace sent a customer notification letter to affected customers,.  The letter identified the affected product problem and actions to be taken.  For questions contact  Customer Support Team at Support.TASE@collins.com",
      "product_quantity": "433 in total",
      "distribution_pattern": "US Nationwide Distribution",
      "openfda": {
        "device_name": "Laser Target Designator",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}