{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Laurel",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77843",
      "recalling_firm": "X-Laser Llc",
      "address_1": "9125 Whiskey Bottom Rd Ste A",
      "address_2": "N/A",
      "postal_code": "20723-1333",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution",
      "recall_number": "Z-2870-2017",
      "product_description": "X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max MKII, X-Beam, Hawk 500    High-power laser light show projector.",
      "product_quantity": "830",
      "reason_for_recall": "Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation",
      "recall_initiation_date": "20170724",
      "center_classification_date": "20170913",
      "termination_date": "20240416",
      "report_date": "20170920",
      "code_info": "LLS projectors"
    }
  ]
}