{
  "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": "Ongoing",
      "city": "Beijing",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79697",
      "recalling_firm": "Beijing Syntech Laser Co., Ltd",
      "address_1": "International Industry Base",
      "address_2": "West Area F/4; No. 8 Liye Road; Changping",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution",
      "recall_number": "Z-1492-2018",
      "product_description": "Beijing Syntech Laser APOLLO V+ Medical Platform     surgical lasers",
      "product_quantity": "11",
      "reason_for_recall": "The noncompliance is that the certification label was not affixed on the product,  with statement  \"Complies with  21 CFR  1040.10 and  1040.11 except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007\".",
      "recall_initiation_date": "20170703",
      "center_classification_date": "20180502",
      "report_date": "20180509",
      "code_info": "Model Apollo V + Medical Platform"
    }
  ]
}