Model Number LNQ11 |
Device Problems
Over-Sensing (1438); Reset Problem (3019)
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Patient Problem
Blood Loss (2597)
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Event Date 05/16/2018 |
Event Type
Injury
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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) patient experienced excessive bleeding at the implant site one day after the device was implanted.Electrical cautery was used for treatment and may have caused the electrical reset to occur.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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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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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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Search Alerts/Recalls
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