{
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          "patient_sequence_number": "1",
          "text": "THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. REPORTED EVENTS: 1 PREVIOUSLY REPORTED EVENT WAS INCLUDED UNDER MFR REPORT # 0001811755-2020-00227 BUT SHOULD BE INCLUDED UNDER THIS REPORT. PRODUCT RETURN STATUS: 1 DEVICE WAS RECEIVED. EVENT CONFIRMATION STATUS: 1 REPORTED EVENT WAS NOT CONFIRMED. EVALUATION RESULTS: 1 DEVICE WAS FOUND TO BE AFFECTED BY A DAMAGED CABLE."
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}