Model Number LNQ11 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Pain (1994)
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Event Date 05/28/2019 |
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 pain.The icm was explanted.No further patient compl ications have been reported as a result of this event.
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Manufacturer Narrative
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Product event summary: the device was returned and analyzed.Returned product analysis was performed and no anomalies were found.If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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