Catalog Number CS-12402 |
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 06/10/2022 |
Event Type
malfunction
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Event Description
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The complaint is reported as: "patient with whom this catheter was going to be used, at the time of performing the test of both routes, they notice that the catheter presents resistance through the proximal route, they try again with another syringe loaded with saline solution and more volume but it continues to present this failure, so it was decided to use another central venous catheter." there was no patient harm 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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The complaint is reported as: "patient with whom this catheter was going to be used, at the time of performing the test of both routes, they notice that the catheter presents resistance through the proximal route, they try again with another syringe loaded with saline solution and more volume but it continues to present this failure, so it was decided to use another central venous catheter." there was no patient harm reported.The patient's condition is reported as fine.
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Search Alerts/Recalls
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