Catalog Number V49663C-25 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Awareness during Anaesthesia (1707)
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Event Date 10/20/2014 |
Event Type
Injury
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Event Description
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A report was received that stated that a patient received insufficient local anesthesia when the suspect medical device was used.It was necessary to place patient under general anesthesia during the procedure.No adverse effects to patient under general anesthesia during the procedure.No adverse effects to patient reported.
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Manufacturer Narrative
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Customer has not yet returned the device to the manufacturer for device evaluation.When and if the device becomes available and is returned and evaluated, the manufacturer will file a follow-up report detailing the results of the evaluation.
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Search Alerts/Recalls
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