{
  "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": "2026-09-08",
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          "patient_problems": [
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        }
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      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
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      "manufacturer_state": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "15539970",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "STERILE PROCESSING DEPT INSPECTED DA VINCI CAUTERY SPATULA AFTER IT WAS USED. FOUND ONE OF THE CABLES ON THE ARTICULATING TIP WAS NO LONGER SEATED PROPERLY AND WAS STICKING OUT."
        }
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      "manufacturer_contact_exchange": "",
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}