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Model Number LNQ11 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Complaint, Ill-Defined (2331)
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Event Date 09/11/2020 |
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's body rejected the implant.The icm was removed.No further patient complications have been reported as a result of this event.
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Search Alerts/Recalls
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