{
  "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": "Beijing",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67520",
      "recalling_firm": "China Daheng Group Inc.",
      "address_1": "#A9 Shangdi Xinxilu",
      "address_2": "Haidian District",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "CA, KS, IL, PA, NJ, WI, WY, KY, FL and NY  India, Indonesia, Turkey, Denmark, and France,",
      "recall_number": "Z-1145-2014",
      "product_description": "Denlase: Diode Laser Therapy System and  Penlase:  Dental Laser Therapy System surgical powered.    Surgical powered Laser instruments.",
      "product_quantity": "238",
      "reason_for_recall": "Failure to provide calibration procedures to purchasers, as required by 21 CFR 1040.11(a)(2).  For example, the user manual did not contain calibration procedures for Denlase or Penlase Lasers",
      "recall_initiation_date": "20130715",
      "center_classification_date": "20140314",
      "termination_date": "20150417",
      "report_date": "20140326",
      "code_info": "Denlase and Penlase Dental  Laser Systems.",
      "more_code_info": ""
    }
  ]
}