{
  "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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          "device_availability": "No answer provided",
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          "device_evaluated_by_manufacturer": "",
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      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20200427",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10000530",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20200420",
      "manufacturer_name": "",
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      "remedial_action": [
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "189012554",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IV CATHETER, SMITHS MEDICAL, LOT #3847475, EXP 2022-07-13. INSERTED INTO VEIN, PULLED BACK ON HOLDING AREA AND LOCK DID NOT ENGAGE (CLICK). BARE NEEDLE EXPOSED TO ME. DID NOT RETRACT AS THEY ARE SUPPOSED TO DO FOR SAFETY. REPORTED TO CHARGE RN. PATIENT WAS NOT IDENTIFIED. NO HARM REPORTED."
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      "suppl_dates_fda_received": ""
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}