Model Number CI24RE (L24) |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Discomfort (2330)
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Event Date 01/22/2021 |
Event Type
Injury
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Manufacturer Narrative
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This report is submitted on february 16, 2021.
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Event Description
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Per the clinic, the device was explanted on (b)(6) 2021, due to the patient experiencing discomfort with device use.The patient was reimplanted with a new device during the same surgery.
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Manufacturer Narrative
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This report is submitted on 14 april 2021.
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Search Alerts/Recalls
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