Catalog Number A3559-25 |
Device Problem
Unknown (for use when the device problem is not known) (2204)
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Patient Problems
Awareness during Anaesthesia (1707); Therapy/non-surgical treatment, additional (2519)
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Event Date 01/20/2014 |
Event Type
Injury
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Event Description
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A report was received that stated that a pt received insufficient local anesthesia when the suspect medical device was used.It was necessary to place an epidural catheter on the pt for use during the procedure.No further adverse effects to pt reported.
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Manufacturer Narrative
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Customer has not yet returned the device to the manufacturer for device eval.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 eval.
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Search Alerts/Recalls
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