Catalog Number EJ-05400-E |
Device Problem
Difficult To Position (1467)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/01/2017 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The facility has communicated that the device is not available for evaluation.The manufacturer will continue to monitor and trend related events.
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Event Description
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The inserted catheter could not be connected with the snaplock adapter.Therefore, the catheter and the snaplock adapter were replaced by new ones.The patient's condition was reported as fine.
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Manufacturer Narrative
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(b)(4).Device history record review was performed on the epidural catheter and snaplock adapter with no relevant findings.A corrective action is not required at this time as a potential 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 and snaplock adapter with no relevant findings.Therefore, the potential cause of the catheter not connecting to the snaplock adapter could not be determined based upon the information provided and without a sample.
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Event Description
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The inserted catheter could not be connected with the snaplock adapter.Therefore, the catheter and the snaplock adapter were replaced by new ones.The patient's condition was reported as fine.
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Search Alerts/Recalls
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