Catalog Number CDC-21242-XN1A |
Device Problem
Obstruction of Flow (2423)
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Patient Problem
Thrombosis/Thrombus (4440)
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Event Date 01/19/2024 |
Event Type
malfunction
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Event Description
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It was reported "when accessing the brown port to obtain a sample for labs, rn had difficulty pulling back, and ended up removing a very large clot from the lumen.The catheter was discontinued, and the patient was transferred to the step-down unit." no patient injury or consequence.No medical intervention required.The patient's current condition is reported as "fine".
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Manufacturer Narrative
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(b)(4).
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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.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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Event Description
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It was reported "when accessing the brown port to obtain a sample for labs, rn had difficulty pulling back, and ended up removing a very large clot from the lumen.The catheter was discontinued, and the patient was transferred to the step-down unit." no patient injury or consequence.No medical intervention required.The patient's current condition is reported as "fine".
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Search Alerts/Recalls
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