Catalog Number 93550 |
Device Problem
Appropriate Term/Code Not Available (3191)
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Patient Problem
Seroma (2069)
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Event Type
Injury
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Manufacturer Narrative
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This report is filed, april 7, 2016.The implanted device remains.
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Event Description
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Per the clinic, the patient developed a seroma at the implant site post implantation.Fluid was drained from the site (date not reported) and the patient was prescribed oral antibiotics (date and duration not reported).The issues have resolved.The implanted device remains.
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Manufacturer Narrative
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Correction: the correct patient identifier is (b)(6); not (b)(6) as previously reported.This report is filed may 2, 2016.The implanted device remains.
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Search Alerts/Recalls
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