Model Number CD2357-40Q |
Device Problem
Over-Sensing (1438)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Type
malfunction
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Manufacturer Narrative
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The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Event Description
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It was reported the patient presented in clinic.Upon interrogation, it was observed the patient's implantable cardiac defibrillator (icd) had non sustained right ventricular oversensing due to post-paced t-wave oversensing.The patient's icd was reprogrammed.The patient was in stable condition.
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Event Description
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New information received notes the clinic and doctor involved in the case.
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Search Alerts/Recalls
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