Model Number CI632 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Swelling/ Edema (4577)
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Event Type
Injury
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Manufacturer Narrative
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This report is submitted on 29 sep 2020.
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Event Description
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Per the clinic, it was reported that the patient administrated with antibiotics due to swelling at the coil site.
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Manufacturer Narrative
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There was an aspiration of the fluid collection at the implant site.This report is submitted on february 12, 2021.
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Search Alerts/Recalls
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