{
  "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/",
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      "date_changed": "20250813",
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      "distributor_city": "",
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      "distributor_state": "",
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      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "1000183",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20080125",
      "manufacturer_name": "",
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      "remedial_action": [
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      "mdr_text": [
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          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "THE PHYSICIAN IMPLANTED A GORE TEX VASCULAR GRAFT (LINED) IN 2007 FOR AV ACCESS. SEROUS LEAKAGE WAS REPORTED AT THE TOP OF THE LOOP OF THE GRAFT SHORTLY AFTER IMPLANT. IN 2007, THE PHYSICIAN REPLACED THE GRAFT DUE TO A SEROMA. ACCORDING TO THE PHYSICIAN THE HYPODERMAL TISSUE OR ADIPOSE OF THE PATIENT'S ARM AT THE IMPLANT SITE WAS NOT ENOUGH."
        },
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          "text": "DEVICE EVALUATION ANTICIPATED, BUT NOT YET COMPLETE. LOT NUMBER UNKNOWN."
        }
      ],
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      "manufacturer_contact_postal_code": "",
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      "manufacturer_contact_pcountry": "",
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    }
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}