Model Number ASKU |
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 october 19, 2020.
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Event Description
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Per the clinic, the patient experienced swelling at the implant site, and was treated with oral steroids.The implanted device remains.
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Manufacturer Narrative
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Correction: this mdr was a duplicate.Any further information will be provided with report number 6000034-2020-03067.This report is submitted on june 23, 2022.
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Search Alerts/Recalls
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