{
  "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": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Dongguan",
      "state": "N/A",
      "country": "China",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97139",
      "recalling_firm": "Flexicare Medical (Dongguan) Ltd.",
      "address_1": "Hengli Town",
      "address_2": "No. B-15 Xicheng; Henglizhen",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of WA, SD, TX, VA, PA, OK, GA, MI, WY, NC, OH.",
      "recall_number": "Z-2185-2025",
      "product_description": "Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle  REF:040-03-0000U",
      "product_quantity": "N/A",
      "reason_for_recall": "Laryngoscope handles may not illuminate as intended.",
      "recall_initiation_date": "20250711",
      "center_classification_date": "20250801",
      "report_date": "20250813",
      "code_info": "Lots: 2007xxxxx to 2012xxxxx (July-2020 to Dec-2020)",
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}