{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94125",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: OUS Only;  International distribution in the states of Australia, Chile, Germany, Hong Kong, Japan, New Zealand and Singapore.",
      "recall_number": "Z-1385-2024",
      "product_description": "SOLTIVE Premium SuperPulsed Laser (TFL-PLS )",
      "product_quantity": "203 Units (OUS Only)",
      "reason_for_recall": "A non-compliant power cord may have been supplied in regions that do not utilize the Type B or Type E/F plug configurations.",
      "recall_initiation_date": "20240129",
      "center_classification_date": "20240327",
      "report_date": "20240403",
      "code_info": "Model Number: TFL-PLS; UDI/DI: 00821925044111; All serial numbers.",
      "more_code_info": ""
    }
  ]
}