Catalog Number AB-19608-S |
Device Problem
Difficult to Flush (1251)
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Patient Problem
No Patient Involvement (2645)
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Event Date 03/13/2017 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has not been returned for investigation at this time.Teleflex will continue to monitor and trend related events.
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Event Description
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The catheter could not be flushed.This occurred prior to use on a patient.
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Manufacturer Narrative
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(b)(4).A device history record review was performed on the epidural catheter with no relevant findings.A corrective action is not required at this time as a potential root cause could not be determined based upon the information provided and without a sample.Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed on the catheter with no evidence to suggest a manufacturing related cause.The potential cause of the catheter not being able to flush could not be determined based upon the information provided and without a sample.
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Event Description
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The catheter could not be flushed.This occurred prior to use on a patient.
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Search Alerts/Recalls
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