Model Number LNQ11 |
Device Problem
Under-Sensing (1661)
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Patient Problems
Syncope (1610); No Known Impact Or Consequence To Patient (2692)
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Event Date 05/27/2018 |
Event Type
malfunction
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that, one hour after the patient experienced a syncopal episode, the implantable cardiac monitor (icm) experienced intermittent undersensing of possible premature ventricular contractions (pvc).It was also noted that the device may have had false classification of bradycardia episodes due to the undersensed pvcs.The device remains in use.No further patient complications have been reported as a result of this event.
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that the implantable cardiac monitor (icm) experienced intermittent undersensing of possible premature ventricular contractions (pvc).It was also noted that the device may have had false classification of bradycardia episodes due to the undersensed pvcs.The device remains in use.No patient complications have been reported as a result of this event.
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Search Alerts/Recalls
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