Model Number 3660 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Abscess (1690); Purulent Discharge (1812)
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Event Date 09/15/2017 |
Event Type
Injury
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Manufacturer Narrative
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Sjm has limited information related to the patient's medical history and is unable to form an opinion as to the relevancy of the patient's history to the event reported.Sjm defers to the patient's physician regarding medical history.
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Event Description
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Device 1 of 2: reference mfr.Report: 1627487-2017-05745.It was reported the patient developed an abscess at the wound site.Further evaluation of the wound is pending.
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Event Description
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Device 1 of 2, reference mfr.Report: 1627487-2017-05745.Follow-up revealed the patient's wound abscess continues to be monitored as it has not completely resolved.
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Event Description
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Device 1 of 2 , reference mfr.Report: 1627487-2017-05745.Follow-up identified the patient's wound site has improved.In addition, the patient is no longer on antibiotics.
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Search Alerts/Recalls
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