{
  "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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      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "",
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      "recall_number": "Z-0278-2024",
      "product_description": "DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.",
      "product_quantity": "2 units",
      "reason_for_recall": "Potential for units suspended on the ceiling to fail and fall.",
      "recall_initiation_date": "20230921",
      "center_classification_date": "20231108",
      "report_date": "20231115",
      "code_info": "Model No. 712026; Serial No. SN14000197 & SN14000260.",
      "more_code_info": ""
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}