{
  "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": "2026-04-01",
    "results": {
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      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84756",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1492-2020",
      "product_description": "UroDiagnost Eleva, system code 708033",
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      "reason_for_recall": "A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.",
      "recall_initiation_date": "20191230",
      "center_classification_date": "20200313",
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      "report_date": "20200325",
      "code_info": "Serial numbers  64  48  2  60",
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}