{
  "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": {
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      "status": "Ongoing",
      "city": "New York",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86706",
      "recalling_firm": "Inova Lasers LLC",
      "address_1": "433 5th Ave Fl 6",
      "address_2": "N/A",
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      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0440-2021",
      "product_description": "Class IV New Era medical laser device",
      "product_quantity": "8 units",
      "reason_for_recall": "The firm failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standard and certification.",
      "recall_initiation_date": "20200129",
      "center_classification_date": "20201117",
      "report_date": "20201125",
      "code_info": "New Era laser units"
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}