Catalog Number VASCULAR UNKNOWN |
Device Problem
Obstruction of Flow (2423)
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Patient Problem
Insufficient Information (4580)
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Event Date 03/11/2023 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).
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Event Description
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It was reported that: incident occured on (b)(6) 2023.1 day after surgery, the arterial catheter (inserted on (b)(6) was no longer functional.It was impossible to get a reliable wave curve and to sample blood.Blood sampling was performed with a peripheral line and the arterial catheter was removed.
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Event Description
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It was reported that: incident occured on (b)(6) 2023.1 day after surgery, the arterial catheter (inserted on (b)(6) was no longer functional.It was impossible to get a reliable wave curve and to sample blood.Blood sampling was performed with a peripheral line and the arterial catheter was removed.
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Manufacturer Narrative
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Qn#(b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.
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Search Alerts/Recalls
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