{
  "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": "Terminated",
      "city": "Tarrytown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84568",
      "recalling_firm": "Aerolase Corporation",
      "address_1": "777 Old Saw Mill River Rd Ste 205",
      "address_2": "N/A",
      "postal_code": "10591-6703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0769-2020",
      "product_description": "LightPod Neo Lasers",
      "product_quantity": "649",
      "reason_for_recall": "This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device",
      "recall_initiation_date": "20190801",
      "center_classification_date": "20200103",
      "termination_date": "20210330",
      "report_date": "20200115",
      "code_info": "LightPod Neo Lasers"
    }
  ]
}