Model Number LNQ11 |
Device Problem
Migration or Expulsion of Device (1395)
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Patient Problem
Discomfort (2330)
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Event Date 02/24/2016 |
Event Type
malfunction
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Manufacturer Narrative
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The information submitted reflects all relevant data received.If additional relevant information is received, a supplemental report will be submitted.(b)(4).
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Event Description
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It was reported by the patient that they are feeling discomfort from their implantable cardiac monitor (icm) and has been feeling the device move.The device remains in use.No 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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Search Alerts/Recalls
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