{
  "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/",
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    "last_updated": "2026-09-08",
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          "manufacturer_d_address_2": "",
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          "device_evaluated_by_manufacturer": "",
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          "udi_public": "",
          "openfda": {
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      "date_changed": "20250827",
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          "sequence_number_treatment": [
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          "patient_age": "59 YR",
          "patient_sex": "",
          "patient_weight": "86",
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          "patient_problems": [
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            "No Known Impact Or Consequence To Patient"
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        }
      ],
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      "date_report": "20200116",
      "initial_report_to_fda": "",
      "distributor_state": "",
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      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "9616158",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "manufacturer_name": "",
      "report_source_code": "Voluntary report",
      "remedial_action": [
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      "manufacturer_state": "",
      "distributor_address_2": "",
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      "single_use_flag": "",
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      "mdr_text": [
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          "mdr_text_key": "176076692",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "MAKO ROBOTIC EQUIPMENT MADE INCORRECT POSTERIOR CHAMBER CUT DURING SURGERY. FDA SAFETY REPORT ID# (B)(4)."
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
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}