Catalog Number CS-15402-E |
Device Problem
Obstruction of Flow (2423)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/22/2023 |
Event Type
malfunction
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Event Description
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It was reported "a lumen from the catheter didn't have return, was necessary to use another catheter".No patient harm was reported.The patient's 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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(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 "a lumen from the catheter didn't have return, was necessary to use another catheter".No patient harm was reported.The patient's condition is reported as fine.
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Search Alerts/Recalls
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