Catalog Number ASK-05500-HC |
Device Problems
Material Puncture/Hole (1504); Material Twisted/Bent (2981)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 08/09/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has not been returned for investigation.Teleflex will continue to monitor and trend related events.
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Event Description
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It was reported that when the doctor used the catheter in the epidural tray, it became kinked and had a hole in the catheter.The doctor and team did not save the catheter.
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Event Description
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It was reported that when the doctor used the catheter in the epidural tray, it became kinked and had a hole in the catheter.The doctor and team did not save the catheter.
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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 epidural catheter with no relevant findings.The potential cause of this complaint could not be determined based upon the information provided and without a sample.
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Search Alerts/Recalls
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