Model Number LNQ11 |
Device Problems
Premature Discharge of Battery (1057); Nonstandard Device (1420)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 08/28/2017 |
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 the implantable cardiac monitor (icm) device reached recommended replacement time (rrt) earlier than expected.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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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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