{
  "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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    {
      "status": "Ongoing",
      "city": "Reedsville",
      "state": "PA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97217",
      "recalling_firm": "Philips Ultrasound, Inc",
      "address_1": "1 Echo Dr",
      "address_2": "",
      "postal_code": "17084-8603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2361-2025",
      "product_description": "C9-3io Transducer Probe",
      "product_quantity": "171,322 units",
      "reason_for_recall": "To provide clarification and labelling to define the useful life of ultrasound transducers in the field.",
      "recall_initiation_date": "20250703",
      "center_classification_date": "20250822",
      "report_date": "20250903",
      "code_info": "Model No. 989605395612; UDI: (01)00884838061538(21)B2CYBN, (01)00884838061538(21)B0WM4Z, (01)00884838061538(21)B0WM4P; Serial No. B2CYBN, B0WM4Z, B0WM4P.",
      "more_code_info": ""
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}