Catalog Number CS-15402-E |
Device Problems
Material Separation (1562); Material Deformation (2976)
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Patient Problems
No Known Impact Or Consequence To Patient (2692); Device Embedded In Tissue or Plaque (3165); No Information (3190)
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Event Date 06/26/2020 |
Event Type
malfunction
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Manufacturer Narrative
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Qn#: (b)(4).
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Event Description
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At the time of passing the central catheter the guide is deformed and part of it remains in the patient.The piece of guide that was left inside the patient was recovered.
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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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At the time of passing the central catheter the guide is deformed and part of it remains in the patient.The piece of guide that was left inside the patient was recovered.
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Search Alerts/Recalls
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