{
  "meta": {
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    "terms": "https://open.fda.gov/terms/",
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      "mdr_report_key": "1000814",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20080201",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
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      "mdr_text": [
        {
          "mdr_text_key": "780208",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "CT TECHNOLOGIST REPORTED ON 02/04/2008 THAT SHE WAS PREPARING THE ROOM FOR THE START OF MORNING PROCEDURES. AS SHE REACHED FOR THE INJECTOR TO POSITION IT NEXT TO THE PROCEDURE TABLE, SHE HEARD A SNAPPING SOUND AND REALIZED THAT THE INJECTOR WAS FALLING. THE CT TECHNOLOGIST REPORTED THAT SHE CAUGHT THE INJECTOR AND HELD IT UP WHILE ANOTHER STAFF MEMBER POSITIONED A PROCEDURE TABLE UNDER THE INJECTOR TO SUPPORT IT. SHE REPORTED THAT NO PATIENTS WERE IN THE ROOM AT THE TIME OF THE EVENT AND SHE, HERSELF WAS NOT INJURED."
        },
        {
          "mdr_text_key": "7946265",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "FSE REPLACED ARM AND J-BOW BRACKET ASSEMBLY. ADJUSTED HEIGHT AND BALANCE, PERFORMED OPERATIONAL CHECKOUT PROCEDURES, AND VERIFIED OPERATION. THE BROKEN SUSPENSION ARM AND BRACKET (J-BOW) WAS RETURNED TO LIEBEL FLARSHEIM WHERE THE PRODUCT ENGINEER DETERMINED THAT THE BREAK OCCURRED AT THE WELD OF THE FIRST ARM SECTION NEAREST THE J-BOW."
        }
      ],
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      "manufacturer_g1_address_1": "",
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      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}