Catalog Number CV-15703 |
Device Problems
Bent (1059); Difficult to Advance (2920)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/14/2018 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).
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Event Description
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The customer reports: when inserting the catheter, the guide is bent in its distal part, it is possible to pass the catheter with difficulty due to the damage in the guide.Radiography is performed and catheter is demonstrated in a suitable position.
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.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 customer reports: when inserting the catheter, the guide is bent in its distal part, it is possible to pass the catheter with difficulty due to the damage in the guide.Radiography is performed and catheter is demonstrated in a suitable position.
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Search Alerts/Recalls
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