{
  "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": "Ongoing",
      "city": "Westford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82988",
      "recalling_firm": "COLLINS AEROSPACE",
      "address_1": "9 Technology Park Dr",
      "address_2": "N/A",
      "postal_code": "01886-3141",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1783-2019",
      "product_description": "TASE 400 Imaging systems",
      "product_quantity": "433 in total",
      "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.",
      "recall_initiation_date": "20190129",
      "center_classification_date": "20190627",
      "report_date": "20190703",
      "code_info": "TASE 400"
    }
  ]
}