{
  "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": "2026-07-08",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94964",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Canada, Chile, Germany, Hong Kong, Japan, Singapore.",
      "recall_number": "Z-2504-2024",
      "product_description": "Soltive Premium SuperPulsed Laser System, Model TFL-PLS",
      "product_quantity": "1,585 Units",
      "reason_for_recall": "Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.",
      "recall_initiation_date": "20240531",
      "center_classification_date": "20240805",
      "report_date": "20240814",
      "code_info": "Model: TFL-PLS; UDI-DI: 00821925044111; Serial Numbers: All Serial Numbers.",
      "more_code_info": ""
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}