Catalog Number CU-25122-F |
Device Problem
Complete Blockage (1094)
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Patient Problems
Thrombus (2101); No Known Impact Or Consequence To Patient (2692)
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Event Date 05/09/2019 |
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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The customer reports that the doctor found a thrombus which blocked the catheter during use.The device was replaced.
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Event Description
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The customer reports that the doctor found a thrombus which blocked the catheter during use.The device was replaced.
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed and no relevant findings were identified.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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