Catalog Number CS-14502 |
Device Problem
Migration or Expulsion of Device (1395)
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Patient Problem
Insufficient Information (4580)
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Event Date 08/24/2022 |
Event Type
malfunction
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Event Description
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The complaint is reported as: patient who is stable at the moment, without requiring aminergic support, dobutamine is suspended after the accidental removal of the central venous catheter by the patient despite having gentle support, central venous catheter is placed again.Additional information was requested but was not available at the time of this report.
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Manufacturer Narrative
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Qn# (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 who is stable at the moment, without requiring aminergic support, dobutamine is suspended after the accidental removal of the central venous catheter by the patient despite having gentle support, central venous catheter is placed again.Additional information was requested but was not available at the time of this report.
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Search Alerts/Recalls
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