{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Alameda",
      "address_1": "1660 S Loop Rd",
      "reason_for_recall": "It has been determined that a lot of fiber lasers were programmed incorrectly. As a result, the fibers from this lot will produce an error and will not allow the user to use the laser when it is plugged in.",
      "address_2": "",
      "product_quantity": "45 lasers",
      "code_info": "Lot # 21144, Use by 08/10/2021",
      "center_classification_date": "20191018",
      "distribution_pattern": "PA and VA",
      "state": "CA",
      "product_description": "OptiLITE, Products for Laser Surgery, Model # CGH1080F, 800 micron single-use holmium fiber assembly with flat tip, Lot Number 21144, Sterilized by Sterrad Run 4149, This device is for single-use only, sterile,  UDI: 00855430006036",
      "report_date": "20191030",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Xintec Corp",
      "recall_number": "Z-0162-2020",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "83902",
      "termination_date": "20210428",
      "more_code_info": "",
      "recall_initiation_date": "20171029",
      "postal_code": "94502-7091",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}