Model Number 3662 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Abscess (1690)
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Event Date 07/10/2019 |
Event Type
Injury
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Manufacturer Narrative
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Further information was requested but not received.
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Event Description
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Related manufacturer report number 1627487-2019-08354.It was reported that patient had an abscess with a bloody discharge issue.It is unknown when this issue began.Patient requested for a magnetic resonance imaging (mri) diagnosis.No further information is available.
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Manufacturer Narrative
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The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
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Event Description
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Related manufacturer report number 1627487-2019-08354.
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Search Alerts/Recalls
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