{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Colorado Springs",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90364",
      "recalling_firm": "Spectranetics Corporation",
      "address_1": "9965 Federal Dr",
      "address_2": "",
      "postal_code": "80921-3822",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US: AR\tAZ\tCA\tCO\tCT\tFL\tGA\tHI\tIA\tIL\tIN\tKS\tLA\tMA\tMD\tME\tMI\tMN\tMO\tNC\tNJ\tNY\tOK\tPA\tTN\tTX\tVA  OUS: Saudi Arabia, Denmark, France, Greece, India, Italy, Netherlands, Serbia, Spain, Sweden, United Kingdom",
      "recall_number": "Z-1351-2022",
      "product_description": "Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM",
      "product_quantity": "105 units",
      "reason_for_recall": "The LAS-100 Laser system may detect an inoperable hardware component during power up, which results in an error code and the system not being operable until code is cleared.",
      "recall_initiation_date": "20220601",
      "center_classification_date": "20220711",
      "report_date": "20220720",
      "code_info": "Serial Numbers: 100000  to 100104 UDI/DI: (01)00813132027452",
      "more_code_info": ""
    }
  ]
}