{
  "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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          "manufacturer_d_address_2": "BLDG 101",
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          "manufacturer_d_country": "US",
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          "sequence_number_treatment": [
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      "manufacturer_g1_country": "",
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      "mdr_report_key": "2396742",
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      "number_devices_in_event": "",
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      "report_source_code": "Voluntary report",
      "remedial_action": [
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      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "N",
      "distributor_address_1": "",
      "manufacturer_state": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "2401329",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "A PIECE OF THE WORKING ELEMENT ON A PERMANENT CAUTERY SPATULA BEING USED IN THE O.R. BROKE OFF INSIDE THE ABDOMEN DURING A PROCEDURE. PIECE WAS VISUALIZED AND REMOVED. CASE CONTINUED WITH A NEW DEVICE."
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      "manufacturer_contact_exchange": "",
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    }
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}