{
  "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",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide domestic distribution. Foreign distribution worldwide.",
      "recall_number": "Z-1490-2020",
      "product_description": "OmniDiagnost Eleva System codes 708028  708027",
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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",
      "termination_date": "20221117",
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      "code_info": "Serial codes  152  49      514  179  611  C@23273  46  560  555  464  14  90  198  15  326  143*003  451  267  FR90-111  417  59  390  164  135  23  143  80  219  24  78  73  15  79  109  624  71  44  576  70  460  62  98  63  620  147  100  68  122  422  12  54  490  97  138  20  130  67  ON100031011SN273  241  435  125  89  47  17  33  134  574",
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