{
  "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": "Louisville",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83302",
      "recalling_firm": "ASTRA, LLC",
      "address_1": "282 Century Lane",
      "address_2": "N/A",
      "postal_code": "80027",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2100-2019",
      "product_description": "Lidar System for Erosion Flume Application  Class 1 Laser Product    Product Usage:  Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access",
      "product_quantity": "1 product",
      "reason_for_recall": "Failure to comply event due to incorrect labeling of a class 1 laser product.",
      "recall_initiation_date": "20190425",
      "center_classification_date": "20190807",
      "report_date": "20190814",
      "code_info": "Model: L1, identified by Accession No. RH19A0069"
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}